A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553558



Internal ID15994281
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+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1661n54
Supporting Variantsnssv768267, nssv768269, nssv768268, nssv768270, nssv768271, nssv768272
Samples
Known GenesRRAS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553558
Frequency
Sample Size17421
Observed Gain4
Observed Loss2
Observed Complex0
Frequencyn/a


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