A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv768266



Internal ID15715536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14358520..14359268hg38UCSC Ensembl
Innerchr11:14380066..14380814hg19UCSC Ensembl
Innerchr11:14336642..14337390hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38749
hg19749
hg18749
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553557
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)nssv768266
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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