A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021032



Internal ID19110250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:79236833..79311751hg38UCSC Ensembl
Innerchr8:80149068..80223986hg19UCSC Ensembl
Innerchr8:80311623..80386541hg18UCSC Ensembl
Cytoband8q21.13
Allele length
AssemblyAllele length
hg3874919
hg1974919
hg1874919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7244n100
Supporting Variantsnssv3689585
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)nsv1021032
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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