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nsv5525329

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:4,285

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 250 SVs from 37 studies. See in: genome view    
Submitted genomic81,238,948-81,243,232Question Mark
Overlapping variant regions from other studies: 248 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):79,212,748-79,217,032Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5525329Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1781,238,94881,243,232
nsv5525329RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1779,212,74879,217,032

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17715562deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17715562Submitted genomicNC_000017.11:g.812
38948_81243232del
GRCh38 (hg38)NC_000017.11Chr1781,238,94881,243,232
nssv17715562RemappedPerfectNC_000017.10:g.792
12748_79217032del
GRCh37.p13First PassNC_000017.10Chr1779,212,74879,217,032

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)
nssv17715562<0.00116404
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