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nsv5425764

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:883

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 169 SVs from 28 studies. See in: genome view    
Submitted genomic175,097,579-175,098,461Question Mark
Overlapping variant regions from other studies: 171 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):175,066,715-175,067,597Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5425764Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr1175,097,579175,098,461
nsv5425764RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr1175,066,715175,067,597

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16892260deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16892260Submitted genomicNC_000001.11:g.175
097579_175098461de
l
GRCh38 (hg38)NC_000001.11Chr1175,097,579175,098,461
nssv16892260RemappedPerfectNC_000001.10:g.175
066715_175067597de
l
GRCh37.p13First PassNC_000001.10Chr1175,066,715175,067,597

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)
nssv16892260<0.00136404
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