A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891177



Internal ID19185573
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:110482693..110641971hg38UCSC Ensembl
Outerchr7:110482693..110641971hg38UCSC Ensembl
Innerchr7:110122750..110282027hg19UCSC Ensembl
Outerchr7:110122750..110282027hg19UCSC Ensembl
Innerchr7:109909986..110069263hg18UCSC Ensembl
Outerchr7:109909986..110069263hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38159279
hg19159278
hg18159278
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25798001
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891177
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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