A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695902



Internal ID15085868
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:120169734..120239258hg38UCSC Ensembl
Innerchr11:120040442..120109967hg19UCSC Ensembl
Innerchr11:119545652..119615177hg18UCSC Ensembl
Innerchr11:119545652..119615177hg17UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3869525
hg1969526
hg1869526
hg1769526
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518464
Supporting Variants
Samples
Known GenesOAF, POU2F3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695902
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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