A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703982



Internal ID15093948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:46911729..46952058hg38UCSC Ensembl
Innerchr19:47414986..47455315hg19UCSC Ensembl
Innerchr19:52106826..52147155hg18UCSC Ensembl
Innerchr19:52106826..52147155hg17UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg3840330
hg1940330
hg1840330
hg1740330
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520664
Supporting Variants
Samples
Known GenesARHGAP35
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703982
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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