A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679215



Internal ID15069181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:45881643..45943578hg38UCSC Ensembl
Innerchr11:45903194..45965129hg19UCSC Ensembl
Innerchr11:45859770..45921705hg18UCSC Ensembl
Innerchr11:45859770..45921705hg17UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg3861936
hg1961936
hg1861936
hg1761936
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516442
Supporting Variants
Samples
Known GenesC11orf94, CRY2, GYLTL1B, MAPK8IP1, PEX16, PHF21A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679215
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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