A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7316n100



Internal ID22793403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:131946693..131986465hg38UCSC Ensembl
chr8:132958940..132998712hg19UCSC Ensembl
chr8:133028122..133067894hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3839773
hg1939773
hg1839773
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1018399, nsv1034614
Samples
Known GenesEFR3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7316n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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