A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555602



Internal ID15996325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:82886203..82980910hg38UCSC Ensembl
Innerchr11:82597245..82691952hg19UCSC Ensembl
Innerchr11:82274893..82369600hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3894708
hg1994708
hg1894708
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv779844
Samples
Known GenesC11orf82, PRCP, RAB30
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555602
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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