A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683100



Internal ID15419752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:90739547..90861031hg38UCSC Ensembl
Innerchr11:90472715..90594199hg19UCSC Ensembl
Innerchr11:90112363..90233847hg18UCSC Ensembl
Innerchr11:90112363..90233847hg17UCSC Ensembl
Cytoband11q14.3
Allele length
AssemblyAllele length
hg38121485
hg19121485
hg18121485
hg17121485
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521151
Supporting Variants
Samples
Known GenesDISC1FP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683100
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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