A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026533



Internal ID19115751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:82655117..82851274hg38UCSC Ensembl
Innerchr8:83567352..83763509hg19UCSC Ensembl
Innerchr8:83729907..83926064hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg38196158
hg19196158
hg18196158
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757301, nssv3689591
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)nsv1026533
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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