A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv771059



Internal ID15718329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:34622233..34759389hg38UCSC Ensembl
Innerchr11:34643780..34780936hg19UCSC Ensembl
Innerchr11:34600356..34737512hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg38137157
hg19137157
hg18137157
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv554000
Supporting Variants
Samples
Known GenesEHF
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv771059
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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