A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv784584



Internal ID16078540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:116405369..116420117hg38UCSC Ensembl
Innerchr11:116276086..116290834hg19UCSC Ensembl
Innerchr11:115781296..115796044hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3814749
hg1914749
hg1814749
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556449
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)nssv784584
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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