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nsv5563669

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:52

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 84 SVs from 18 studies. See in: genome view    
Submitted genomic65,039,843-65,039,894Question Mark
Overlapping variant regions from other studies: 84 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):65,506,561-65,506,612Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5563669Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000014.9Chr1465,039,84365,039,894
nsv5563669RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000014.8Chr1465,506,56165,506,612

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17696758sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17696758Submitted genomicNC_000014.9:g.6503
9843_65039894ins10
82
GRCh38 (hg38)NC_000014.9Chr1465,039,84365,039,894
nssv17696758RemappedPerfectNC_000014.8:g.6550
6561_65506612ins10
82
GRCh37.p13First PassNC_000014.8Chr1465,506,56165,506,612

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)
nssv17696758<0.00126402
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