A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020406



Internal ID19109625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:134062954..134081206hg38UCSC Ensembl
Innerchr8:135075197..135093449hg19UCSC Ensembl
Innerchr8:135144379..135162631hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3818253
hg1918253
hg1818253
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3692717
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)nsv1020406
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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