A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020007



Internal ID19109226
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:77109140..77147598hg38UCSC Ensembl
Innerchr8:78021376..78059834hg19UCSC Ensembl
Innerchr8:78183931..78222389hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3838459
hg1938459
hg1838459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3757298
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)nsv1020007
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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