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nsv184

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:48,256

Genome View

Select assembly:
Overlapping variant regions from other studies: 1071 SVs from 84 studies. See in: genome view    
Remapped(Score: Perfect):1,570,746-1,619,001Question Mark
Overlapping variant regions from other studies: 1071 SVs from 84 studies. See in: genome view    
Remapped(Score: Perfect):1,551,392-1,599,647Question Mark
Overlapping variant regions from other studies: 12 SVs from 8 studies. See in: genome view    
Submitted genomic1,499,392-1,547,647Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrOuter StartOuter Stop
nsv184RemappedPerfectGRCh38.p12Primary AssemblyFirst PassNC_000020.11Chr201,570,7461,619,001
nsv184RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000020.10Chr201,551,3921,599,647
nsv184Submitted genomicNCBI35 (hg17)Primary AssemblyNC_000020.9Chr201,499,3921,547,647

Variant Call Information

Variant Call IDTypeSample IDMethodAnalysisOther Calls in this Sample and Study
nssv184deletionSAMN00000376SequencingPaired-end mapping297

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrOuter StartOuter Stop
nssv184RemappedPerfectNC_000020.11:g.(15
70746_?)_(?_161900
1)del
GRCh38.p12First PassNC_000020.11Chr201,570,7461,619,001
nssv184RemappedPerfectNC_000020.10:g.(15
51392_?)_(?_159964
7)del
GRCh37.p13First PassNC_000020.10Chr201,551,3921,599,647
nssv184Submitted genomicNC_000020.9:g.(149
9392_?)_(?_1547647
)del33537
NCBI35 (hg17)NC_000020.9Chr201,499,3921,547,647

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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