A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7682n100



Internal ID22793769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:77154478..77180761hg38UCSC Ensembl
chr9:79769394..79795677hg19UCSC Ensembl
chr9:78959214..78985497hg18UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3826284
hg1926284
hg1826284
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046657, nsv1053136, nsv1053065, nsv1049716, nsv1047163, nsv1046262, nsv1051122, nsv1037475
Samples
Known GenesVPS13A, VPS13A-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7682n100
Frequency
Sample Size11257
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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