A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694251



Internal ID15430903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:86325913..86328044hg38UCSC Ensembl
Innerchr11:86036955..86039086hg19UCSC Ensembl
Innerchr11:85714603..85716734hg18UCSC Ensembl
Innerchr11:85714603..85716734hg17UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg382132
hg192132
hg182132
hg172132
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518588
Supporting Variants
Samples
Known GenesC11orf73
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694251
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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