A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3689566



Internal ID18987847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:74186209..74215475hg38UCSC Ensembl
Innerchr8:75098444..75127710hg19UCSC Ensembl
Innerchr8:75260998..75290264hg18UCSC Ensembl
Cytoband8q21.11
Allele length
AssemblyAllele length
hg3829267
hg1929267
hg1829267
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028603
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)nssv3689566
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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