A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768269



Internal ID15715539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14358571..14359260hg38UCSC Ensembl
Innerchr11:14380117..14380806hg19UCSC Ensembl
Innerchr11:14336693..14337382hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38690
hg19690
hg18690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553558
Supporting Variants
Samples
Known GenesRRAS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv768269
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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