A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698160



Internal ID15434812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:5178313..5202814hg38UCSC Ensembl
Innerchr19:5178324..5202825hg19UCSC Ensembl
Innerchr19:5129324..5153825hg18UCSC Ensembl
Innerchr19:5129324..5153825hg17UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3824502
hg1924502
hg1824502
hg1724502
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521544
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698160
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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