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nsv5407372

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

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 212 SVs from 45 studies. See in: genome view    
Submitted genomic175,103,579-175,103,617Question Mark
Overlapping variant regions from other studies: 214 SVs from 45 studies. See in: genome view    
Remapped(Score: Perfect):175,072,715-175,072,753Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5407372Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1175,103,579175,103,617
nsv5407372RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1175,072,715175,072,753

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16891970alu insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16891970Submitted genomicNC_000001.11:g.175
103579_175103617in
s269
GRCh38 (hg38)NC_000001.11Chr1175,103,579175,103,617
nssv16891970RemappedPerfectNC_000001.10:g.175
072715_175072753in
s269
GRCh37.p13First PassNC_000001.10Chr1175,072,715175,072,753

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)
nssv168919700.01656404
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