A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528623



Internal ID15109230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:76450345..76457175hg38UCSC Ensembl
Innerchr11:76161389..76168219hg19UCSC Ensembl
Innerchr11:75839037..75845867hg18UCSC Ensembl
Innerchr11:75839037..75845867hg17UCSC Ensembl
Cytoband11q13.5
Allele length
AssemblyAllele length
hg386831
hg196831
hg186831
hg176831
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705253
Samples
Known GenesC11orf30
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528623
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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