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nsv5563927

  • 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: 198 SVs from 39 studies. See in: genome view    
Submitted genomic47,576,896-47,576,947Question Mark
Overlapping variant regions from other studies: 196 SVs from 39 studies. See in: genome view    
Remapped(Score: Perfect):45,654,262-45,654,313Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5563927Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000017.11Chr1747,576,89647,576,947
nsv5563927RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000017.10Chr1745,654,26245,654,313

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17713503sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17713503Submitted genomicNC_000017.11:g.475
76896_47576947ins1
200
GRCh38 (hg38)NC_000017.11Chr1747,576,89647,576,947
nssv17713503RemappedPerfectNC_000017.10:g.456
54262_45654313ins1
200
GRCh37.p13First PassNC_000017.10Chr1745,654,26245,654,313

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)
nssv17713503<0.00116404
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