A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv785111



Internal ID16079067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:130906629..131144852hg38UCSC Ensembl
Innerchr11:130776524..131014747hg19UCSC Ensembl
Innerchr11:130281734..130519957hg18UCSC Ensembl
Cytoband11q24.3
Allele length
AssemblyAllele length
hg38238224
hg19238224
hg18238224
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556575
Supporting Variants
Samples
Known GenesSNX19
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv785111
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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