A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv777174



Internal ID15724444
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:65498698..65519780hg38UCSC Ensembl
Innerchr11:65266169..65287251hg19UCSC Ensembl
Innerchr11:65022745..65043827hg18UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3821083
hg1921083
hg1821083
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv555210
Supporting Variants
Samples
Known GenesMALAT1, MIR548AR, MIR548BA
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv777174
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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