A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1114092



Internal ID15967278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:45927486..45937627hg38UCSC Ensembl
Innerchr8:46839108..46849249hg19UCSC Ensembl
Innerchr8:46958273..46968414hg18UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3810142
hg1910142
hg1810142
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611217
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)nssv1114092
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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