A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv778986



Internal ID16072942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:71590143..71719424hg38UCSC Ensembl
Innerchr11:71301189..71430470hg19UCSC Ensembl
Innerchr11:70978837..71108118hg18UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38129282
hg19129282
hg18129282
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555403
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv778986
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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