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nsv5494576

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,828

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 154 SVs from 41 studies. See in: genome view    
Submitted genomic75,051,861-75,056,688Question Mark
Overlapping variant regions from other studies: 154 SVs from 41 studies. See in: genome view    
Remapped(Score: Perfect):75,518,564-75,523,391Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5494576Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1475,051,86175,056,688
nsv5494576RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1475,518,56475,523,391

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17699330deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17699330Submitted genomicNC_000014.9:g.7505
1861_75056688del
GRCh38 (hg38)NC_000014.9Chr1475,051,86175,056,688
nssv17699330RemappedPerfectNC_000014.8:g.7551
8564_75523391del
GRCh37.p13First PassNC_000014.8Chr1475,518,56475,523,391

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)
nssv17699330<0.00116404
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