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nsv5529823

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,782

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 124 SVs from 35 studies. See in: genome view    
Submitted genomic59,282,822-59,286,603Question Mark
Overlapping variant regions from other studies: 124 SVs from 35 studies. See in: genome view    
Remapped(Score: Perfect):59,575,021-59,578,802Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5529823Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000015.10Chr1559,282,82259,286,603
nsv5529823RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000015.9Chr1559,575,02159,578,802

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17700951deletionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17700951Submitted genomicNC_000015.10:g.592
82822_59286603del
GRCh38 (hg38)NC_000015.10Chr1559,282,82259,286,603
nssv17700951RemappedPerfectNC_000015.9:g.5957
5021_59578802del
GRCh37.p13First PassNC_000015.9Chr1559,575,02159,578,802

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)
nssv17700951<0.00116404
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