A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553989



Internal ID16341398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31705684..31775012hg38UCSC Ensembl
Innerchr11:31727232..31796560hg19UCSC Ensembl
Innerchr11:31683808..31753136hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3869329
hg1969329
hg1869329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv771047
Samples
Known GenesELP4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553989
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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