A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553560



Internal ID15994283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:14358623..14359268hg38UCSC Ensembl
Innerchr11:14380169..14380814hg19UCSC Ensembl
Innerchr11:14336745..14337390hg18UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38646
hg19646
hg18646
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1661n54
Supporting Variantsnssv768274, nssv768275
Samples
Known GenesRRAS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553560
Frequency
Sample Size17421
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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