A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555607



Internal ID16343016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:83880541..83909897hg38UCSC Ensembl
Innerchr11:83591584..83620940hg19UCSC Ensembl
Innerchr11:83269232..83298588hg18UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg3829357
hg1929357
hg1829357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1176185
Samples1780854279_A
Known GenesDLG2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555607
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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