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nsv4375620

  • Variant Calls:2
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:722,008

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 5997 SVs from 121 studies. See in: genome view    
Remapped(Score: Good):22,194,192-22,916,199Question Mark
Overlapping variant regions from other studies: 6032 SVs from 121 studies. See in: genome view    
Submitted genomic22,548,592-23,258,369Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrInner StartInner Stop
nsv4375620RemappedGoodGRCh38.p12Primary AssemblyFirst PassNC_000022.11Chr2222,194,19222,916,199
nsv4375620Submitted genomicGRCh37 (hg19)Primary AssemblyNC_000022.10Chr2222,548,59223,258,369

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv15640275copy number loss14-0145-001SNP arrayGenotyping23
nssv15642490copy number loss15-1120-001SNP arrayGenotyping22

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrInner StartInner Stop
nssv15640275RemappedGoodNC_000022.11:g.(?_
22194192)_(2291619
9_?)del
GRCh38.p12First PassNC_000022.11Chr2222,194,19222,916,199
nssv15642490RemappedGoodNC_000022.11:g.(?_
22194192)_(2291619
9_?)del
GRCh38.p12First PassNC_000022.11Chr2222,194,19222,916,199
nssv15640275Submitted genomicNC_000022.10:g.(?_
22548592)_(2325836
9_?)del
GRCh37 (hg19)NC_000022.10Chr2222,548,59223,258,369
nssv15642490Submitted genomicNC_000022.10:g.(?_
22548592)_(2325836
9_?)del
GRCh37 (hg19)NC_000022.10Chr2222,548,59223,258,369

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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