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nsv5528789

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:39,857

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 271 SVs from 43 studies. See in: genome view    
Submitted genomic36,489,215-36,529,071Question Mark
Overlapping variant regions from other studies: 271 SVs from 43 studies. See in: genome view    
Remapped(Score: Perfect):36,980,117-37,019,973Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5528789Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1936,489,21536,529,071
nsv5528789RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1936,980,11737,019,973

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723105deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723105Submitted genomicNC_000019.10:g.364
89215_36529071del
GRCh38 (hg38)NC_000019.10Chr1936,489,21536,529,071
nssv17723105RemappedPerfectNC_000019.9:g.3698
0117_37019973del
GRCh37.p13First PassNC_000019.9Chr1936,980,11737,019,973

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)
nssv17723105<0.00116404
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