A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3692709



Internal ID18990990
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:134049828..134081071hg38UCSC Ensembl
Innerchr8:135062071..135093314hg19UCSC Ensembl
Innerchr8:135131253..135162496hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3831244
hg1931244
hg1831244
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023209
Supporting Variants
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)nssv3692709
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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