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nsv5518534

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:656

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 136 SVs from 28 studies. See in: genome view    
Submitted genomic64,810,888-64,811,543Question Mark
Overlapping variant regions from other studies: 136 SVs from 28 studies. See in: genome view    
Remapped(Score: Perfect):62,807,006-62,807,661Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5518534Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1764,810,88864,811,543
nsv5518534RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1762,807,00662,807,661

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17714092deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17714092Submitted genomicNC_000017.11:g.648
10888_64811543del
GRCh38 (hg38)NC_000017.11Chr1764,810,88864,811,543
nssv17714092RemappedPerfectNC_000017.10:g.628
07006_62807661del
GRCh37.p13First PassNC_000017.10Chr1762,807,00662,807,661

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)
nssv17714092<0.00116404
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