A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019832



Internal ID19109050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119315751..119368340hg38UCSC Ensembl
Innerchr8:120327991..120380580hg19UCSC Ensembl
Innerchr8:120397172..120449761hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3852590
hg1952590
hg1852590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757362
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019832
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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