A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891234



Internal ID18838944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149854904..149933638hg38UCSC Ensembl
Outerchr7:149854904..150009836hg38UCSC Ensembl
Innerchr7:149551993..149630727hg19UCSC Ensembl
Outerchr7:149551993..149706925hg19UCSC Ensembl
Innerchr7:149182926..149261660hg18UCSC Ensembl
Outerchr7:149182926..149337858hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38154933
hg19154933
hg18154933
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25787880, essv25788111, essv25788808
Samples
Known GenesATP6V0E2, ATP6V0E2-AS1, ZNF862
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891234
Frequency
Sample Size3017
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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