A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv556471



Internal ID16343880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:119693786..119717352hg38UCSC Ensembl
Innerchr11:119564496..119588062hg19UCSC Ensembl
Innerchr11:119069706..119093272hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg3823567
hg1923567
hg1823567
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1174959
SamplesNINDS_166
Known GenesPVRL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv556471
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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