A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670774



Internal ID15060740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:131775541..131798641hg38UCSC Ensembl
Innerchr11:131645435..131668535hg19UCSC Ensembl
Innerchr11:131150645..131173745hg18UCSC Ensembl
Innerchr11:131150645..131173745hg17UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg3823101
hg1923101
hg1823101
hg1723101
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517550
Supporting Variants
Samples
Known GenesNTM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670774
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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