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nsv5531850

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:34,101

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 612 SVs from 58 studies. See in: genome view    
Submitted genomic16,235,900-16,270,000Question Mark
Overlapping variant regions from other studies: 612 SVs from 58 studies. See in: genome view    
Remapped(Score: Perfect):16,329,757-16,363,857Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5531850Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000016.10Chr1616,235,90016,270,000
nsv5531850RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000016.9Chr1616,329,75716,363,857

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17705049deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17705049Submitted genomicNC_000016.10:g.162
35900_16270000del
GRCh38 (hg38)NC_000016.10Chr1616,235,90016,270,000
nssv17705049RemappedPerfectNC_000016.9:g.1632
9757_16363857del
GRCh37.p13First PassNC_000016.9Chr1616,329,75716,363,857

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Complete genotype and/or allele frequency data for this study can be found on dbVar's FTP site.

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv177050490.1287545888
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