A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555606



Internal ID16343015
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:83256921..83261055hg38UCSC Ensembl
Innerchr11:82967963..82972097hg19UCSC Ensembl
Innerchr11:82645611..82649745hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg384135
hg194135
hg184135
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176184
SamplesHGDP00052
Known GenesCCDC90B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555606
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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