A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1114119



Internal ID15967305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:45931622..45946058hg38UCSC Ensembl
Innerchr8:46843244..46857680hg19UCSC Ensembl
Innerchr8:46962409..46976845hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3814437
hg1914437
hg1814437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611228
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)nssv1114119
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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