A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022540



Internal ID19111758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:72465586..72526835hg38UCSC Ensembl
Innerchr8:73377821..73439070hg19UCSC Ensembl
Innerchr8:73540375..73601624hg18UCSC Ensembl
Cytoband8q13.3
Allele length
AssemblyAllele length
hg3861250
hg1961250
hg1861250
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3689530
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)nsv1022540
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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