A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026655



Internal ID18769186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119270689..119510089hg38UCSC Ensembl
Innerchr8:120282929..120522329hg19UCSC Ensembl
Innerchr8:120352110..120591510hg18UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg38239401
hg19239401
hg18239401
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3691466
Samples
Known GenesNOV
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026655
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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