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nsv5491376

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:74,001

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 289 SVs from 53 studies. See in: genome view    
Submitted genomic45,690,265-45,764,265Question Mark
Overlapping variant regions from other studies: 232 SVs from 45 studies. See in: genome view    
Remapped(Score: Pass):46,185,713-46,224,333Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5491376Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000010.11Chr1045,690,26545,764,265
nsv5491376RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000010.10Chr1046,185,71346,224,333

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv17033556duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv17033556Submitted genomicNC_000010.11:g.456
90265_45764265dup
GRCh38 (hg38)NC_000010.11Chr1045,690,26545,764,265
nssv17033556RemappedPassNC_000010.10:g.461
85713_46224333dup
GRCh37.p13First PassNC_000010.10Chr1046,185,71346,224,333

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)
nssv170335560.00186310
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