A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6752n100



Internal ID22792839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149855445..150054122hg38UCSC Ensembl
chr7:149552534..149751211hg19UCSC Ensembl
chr7:149183467..149382144hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38198678
hg19198678
hg18198678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1017147, nsv1028178, nsv1015591, nsv1016446, nsv1029171
Samples
Known GenesATP6V0E2, ATP6V0E2-AS1, ZNF862
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6752n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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