A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553954



Internal ID16341363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31370402..31382937hg38UCSC Ensembl
Innerchr11:31391949..31404484hg19UCSC Ensembl
Innerchr11:31348525..31361060hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3812536
hg1912536
hg1812536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv770680
Samples
Known GenesDNAJC24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553954
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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