A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1117709



Internal ID15624209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:88748082..89717279hg38UCSC Ensembl
Innerchr8:89760311..90729507hg19UCSC Ensembl
Innerchr8:89829427..90798629hg18UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg38969198
hg19969197
hg18969203
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv611714
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)nssv1117709
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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