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nsv5465192

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:323

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 165 SVs from 31 studies. See in: genome view    
Submitted genomic60,910,670-60,910,992Question Mark
Overlapping variant regions from other studies: 165 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):60,206,497-60,206,819Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5465192Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000005.10Chr560,910,67060,910,992
nsv5465192RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000005.9Chr560,206,49760,206,819

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16967915deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16967915Submitted genomicNC_000005.10:g.609
10670_60910992del
GRCh38 (hg38)NC_000005.10Chr560,910,67060,910,992
nssv16967915RemappedPerfectNC_000005.9:g.6020
6497_60206819del
GRCh37.p13First PassNC_000005.9Chr560,206,49760,206,819

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)
nssv16967915<0.00116404
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