A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704426



Internal ID15441078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:8795148..8835275hg38UCSC Ensembl
Innerchr11:8816695..8856822hg19UCSC Ensembl
Innerchr11:8773271..8813398hg18UCSC Ensembl
Innerchr11:8773271..8813398hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3840128
hg1940128
hg1840128
hg1740128
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527920
Supporting Variants
Samples
Known GenesST5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704426
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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