A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698963



Internal ID15088929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:125945160..125951868hg38UCSC Ensembl
Innerchr11:125815055..125821763hg19UCSC Ensembl
Innerchr11:125320265..125326973hg18UCSC Ensembl
Innerchr11:125320265..125326973hg17UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg386709
hg196709
hg186709
hg176709
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516919
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698963
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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