A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667462



Internal ID15404114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:134706322..134725880hg38UCSC Ensembl
Innerchr11:134576216..134595774hg19UCSC Ensembl
Innerchr11:134081426..134100984hg18UCSC Ensembl
Innerchr11:134081426..134100984hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3819559
hg1919559
hg1819559
hg1719559
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517742
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667462
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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