A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705762



Internal ID15442414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:6822208..6832869hg38UCSC Ensembl
Innerchr19:6822219..6832880hg19UCSC Ensembl
Innerchr19:6773219..6783880hg18UCSC Ensembl
Innerchr19:6773219..6783880hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3810662
hg1910662
hg1810662
hg1710662
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv529046
Supporting Variants
Samples
Known GenesVAV1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705762
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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