A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1115566



Internal ID15968752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:53616200..53676784hg38UCSC Ensembl
Innerchr8:54528760..54589344hg19UCSC Ensembl
Innerchr8:54691313..54751897hg18UCSC Ensembl
Cytoband8q11.23
Allele length
AssemblyAllele length
hg3860585
hg1960585
hg1860585
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611381
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1115566
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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