A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697600



Internal ID15434252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:59079464..59082904hg38UCSC Ensembl
Innerchr15:59371663..59375103hg19UCSC Ensembl
Innerchr15:57158955..57162395hg18UCSC Ensembl
Innerchr15:57158955..57162395hg17UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg383441
hg193441
hg183441
hg173441
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520769
Supporting Variants
Samples
Known GenesRNF111
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697600
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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