A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698816



Internal ID15088782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:133118684..133134341hg38UCSC Ensembl
Innerchr11:132988579..133004236hg19UCSC Ensembl
Innerchr11:132493789..132509446hg18UCSC Ensembl
Innerchr11:132493789..132509446hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3815658
hg1915658
hg1815658
hg1715658
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523117
Supporting Variants
Samples
Known GenesOPCML
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698816
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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