A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv659424



Internal ID15049390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:17282085..17282206hg38UCSC Ensembl
Innerchr19:17392894..17393015hg19UCSC Ensembl
Innerchr19:17253894..17254015hg18UCSC Ensembl
Innerchr19:17253894..17254015hg17UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg38122
hg19122
hg18122
hg17122
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515965
Supporting Variants
Samples
Known GenesANKLE1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv659424
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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