A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6751n100



Internal ID20158367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149855445..149998108hg38UCSC Ensembl
chr7:149552534..149695197hg19UCSC Ensembl
chr7:149183467..149326130hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38142664
hg19142664
hg18142664
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1022103, nsv1035069
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)dgv6751n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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