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nsv5523075

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:6,718

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 184 SVs from 37 studies. See in: genome view    
Submitted genomic36,688,534-36,695,251Question Mark
Overlapping variant regions from other studies: 184 SVs from 37 studies. See in: genome view    
Remapped(Score: Perfect):37,179,436-37,186,153Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5523075Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,688,53436,695,251
nsv5523075RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1937,179,43637,186,153

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723122deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723122Submitted genomicNC_000019.10:g.366
88534_36695251del
GRCh38 (hg38)NC_000019.10Chr1936,688,53436,695,251
nssv17723122RemappedPerfectNC_000019.9:g.3717
9436_37186153del
GRCh37.p13First PassNC_000019.9Chr1937,179,43637,186,153

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)
nssv17723122<0.00116404
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