A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697497



Internal ID15434149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:63070597..63071039hg38UCSC Ensembl
Innerchr11:62838069..62838511hg19UCSC Ensembl
Innerchr11:62594645..62595087hg18UCSC Ensembl
Innerchr11:62594645..62595087hg17UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg38443
hg19443
hg18443
hg17443
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517447
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697497
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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