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nsv5422583

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:468,132

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 1980 SVs from 87 studies. See in: genome view    
Submitted genomic3,821,016-4,289,147Question Mark
Overlapping variant regions from other studies: 1978 SVs from 87 studies. See in: genome view    
Remapped(Score: Pass):3,737,580-4,349,207Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv5422583Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000001.11Chr13,821,0164,289,147
nsv5422583RemappedPassGRCh37.p13Primary AssemblyFirst PassNC_000001.10Chr13,737,5804,349,207

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16903269duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16903269Submitted genomicNC_000001.11:g.382
1016_4289147dup
GRCh38 (hg38)NC_000001.11Chr13,821,0164,289,147
nssv16903269RemappedPassNC_000001.10:g.373
7580_4349207dup
GRCh37.p13First PassNC_000001.10Chr13,737,5804,349,207

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)
nssv16903269<0.00116404
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