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nsv5554586

  • 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: 85 SVs from 18 studies. See in: genome view    
Submitted genomic45,841,689-45,841,740Question Mark
Overlapping variant regions from other studies: 85 SVs from 18 studies. See in: genome view    
Remapped(Score: Perfect):46,344,947-46,344,998Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5554586Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000019.10Chr1945,841,68945,841,740
nsv5554586RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000019.9Chr1946,344,94746,344,998

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17723611sva insertionSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17723611Submitted genomicNC_000019.10:g.458
41689_45841740ins1
290
GRCh38 (hg38)NC_000019.10Chr1945,841,68945,841,740
nssv17723611RemappedPerfectNC_000019.9:g.4634
4947_46344998ins12
90
GRCh37.p13First PassNC_000019.9Chr1946,344,94746,344,998

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)
nssv17723611<0.00126404
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