A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3677438



Internal ID18975719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:6747666..6764806hg38UCSC Ensembl
Innerchr8:6605187..6622327hg19UCSC Ensembl
Innerchr8:6592595..6609737hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3817141
hg1917141
hg1817143
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028963
Supporting Variants
Samples
Known GenesAGPAT5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3677438
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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