A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668447



Internal ID15058413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45881643..45918090hg38UCSC Ensembl
Innerchr11:45903194..45939641hg19UCSC Ensembl
Innerchr11:45859770..45896217hg18UCSC Ensembl
Innerchr11:45859770..45896217hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3836448
hg1936448
hg1836448
hg1736448
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516442
Supporting Variants
Samples
Known GenesC11orf94, CRY2, MAPK8IP1, PEX16
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668447
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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