A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv763436



Internal ID15710706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:403545..408352hg38UCSC Ensembl
Innerchr11:403545..408352hg19UCSC Ensembl
Innerchr11:393545..398352hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg384808
hg194808
hg184808
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552822
Supporting Variants
Samples
Known GenesPKP3, SIGIRR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv763436
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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