A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv660646



Internal ID15397298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134479021..134851577hg38UCSC Ensembl
Innerchr11:134348915..134721471hg19UCSC Ensembl
Innerchr11:133854125..134226681hg18UCSC Ensembl
Innerchr11:133854125..134226681hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38372557
hg19372557
hg18372557
hg17372557
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517742
Supporting Variants
Samples
Known GenesLOC283177
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv660646
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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