A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026966



Internal ID19116184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:85579538..85640901hg38UCSC Ensembl
Innerchr8:86491767..86553130hg19UCSC Ensembl
Innerchr8:86679019..86740382hg18UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3861364
hg1961364
hg1861364
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7256n100
Supporting Variantsnssv3689651
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)nsv1026966
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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