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nsv893084

  • Variant Calls:6
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:94,559

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 677 SVs from 79 studies. See in: genome view    
Remapped(Score: Perfect):39,004,143-39,098,701Question Mark
Overlapping variant regions from other studies: 760 SVs from 83 studies. See in: genome view    
Remapped(Score: Perfect):39,004,140-39,098,698Question Mark
Overlapping variant regions from other studies: 314 SVs from 28 studies. See in: genome view    
Submitted genomic38,994,140-39,088,698Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nsv893084RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000009.12Chr939,004,14339,019,62739,096,46139,098,701
nsv893084RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000009.11Chr939,004,14039,019,62439,096,45839,098,698
nsv893084Submitted genomicNCBI36 (hg18)Primary AssemblyNC_000009.10Chr938,994,14039,009,62439,086,45839,088,698

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv1502225copy number gainSP50857SNP arraySNP genotyping analysis20
nssv1502277copy number gainSP50882SNP arraySNP genotyping analysis24
nssv1509577copy number gainSP54879SNP arraySNP genotyping analysis10
nssv1513141copy number gainSP55690SNP arraySNP genotyping analysis15
nssv1515709copy number gainSP56248SNP arraySNP genotyping analysis25
nssv1516170copy number gainSP56505SNP arraySNP genotyping analysis26

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartInner StartInner StopOuter Stop
nssv1502225RemappedPerfectNC_000009.12:g.(39
004143_39019627)_(
39096461_39098701)
dup		GRCh38.p12First PassNC_000009.12Chr939,004,14339,019,62739,096,46139,098,701
nssv1502277RemappedPerfectNC_000009.12:g.(39
004143_39019627)_(
39096461_39098701)
dup		GRCh38.p12First PassNC_000009.12Chr939,004,14339,019,62739,096,46139,098,701
nssv1509577RemappedPerfectNC_000009.12:g.(39
004143_39019627)_(
39096461_39098701)
dup		GRCh38.p12First PassNC_000009.12Chr939,004,14339,019,62739,096,46139,098,701
nssv1513141RemappedPerfectNC_000009.12:g.(39
004143_39019627)_(
39096461_39098701)
dup		GRCh38.p12First PassNC_000009.12Chr939,004,14339,019,62739,096,46139,098,701
nssv1515709RemappedPerfectNC_000009.12:g.(39
004143_39019627)_(
39096461_39098701)
dup		GRCh38.p12First PassNC_000009.12Chr939,004,14339,019,62739,096,46139,098,701
nssv1516170RemappedPerfectNC_000009.12:g.(39
004143_39019627)_(
39096461_39098701)
dup		GRCh38.p12First PassNC_000009.12Chr939,004,14339,019,62739,096,46139,098,701
nssv1502225RemappedPerfectNC_000009.11:g.(39
004140_39019624)_(
39096458_39098698)
dup		GRCh37.p13First PassNC_000009.11Chr939,004,14039,019,62439,096,45839,098,698
nssv1502277RemappedPerfectNC_000009.11:g.(39
004140_39019624)_(
39096458_39098698)
dup		GRCh37.p13First PassNC_000009.11Chr939,004,14039,019,62439,096,45839,098,698
nssv1509577RemappedPerfectNC_000009.11:g.(39
004140_39019624)_(
39096458_39098698)
dup		GRCh37.p13First PassNC_000009.11Chr939,004,14039,019,62439,096,45839,098,698
nssv1513141RemappedPerfectNC_000009.11:g.(39
004140_39019624)_(
39096458_39098698)
dup		GRCh37.p13First PassNC_000009.11Chr939,004,14039,019,62439,096,45839,098,698
nssv1515709RemappedPerfectNC_000009.11:g.(39
004140_39019624)_(
39096458_39098698)
dup		GRCh37.p13First PassNC_000009.11Chr939,004,14039,019,62439,096,45839,098,698
nssv1516170RemappedPerfectNC_000009.11:g.(39
004140_39019624)_(
39096458_39098698)
dup		GRCh37.p13First PassNC_000009.11Chr939,004,14039,019,62439,096,45839,098,698
nssv1502225Submitted genomicNC_000009.10:g.(38
994140_39009624)_(
39086458_39088698)
dup		NCBI36 (hg18)NC_000009.10Chr938,994,14039,009,62439,086,45839,088,698
nssv1502277Submitted genomicNC_000009.10:g.(38
994140_39009624)_(
39086458_39088698)
dup		NCBI36 (hg18)NC_000009.10Chr938,994,14039,009,62439,086,45839,088,698
nssv1509577Submitted genomicNC_000009.10:g.(38
994140_39009624)_(
39086458_39088698)
dup		NCBI36 (hg18)NC_000009.10Chr938,994,14039,009,62439,086,45839,088,698
nssv1513141Submitted genomicNC_000009.10:g.(38
994140_39009624)_(
39086458_39088698)
dup		NCBI36 (hg18)NC_000009.10Chr938,994,14039,009,62439,086,45839,088,698
nssv1515709Submitted genomicNC_000009.10:g.(38
994140_39009624)_(
39086458_39088698)
dup		NCBI36 (hg18)NC_000009.10Chr938,994,14039,009,62439,086,45839,088,698
nssv1516170Submitted genomicNC_000009.10:g.(38
994140_39009624)_(
39086458_39088698)
dup		NCBI36 (hg18)NC_000009.10Chr938,994,14039,009,62439,086,45839,088,698

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

No genotype data were submitted for this variant

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