A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3891022



Internal ID19185418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4437381..4578519hg38UCSC Ensembl
Outerchr7:4332964..4602171hg38UCSC Ensembl
Innerchr7:4477012..4618150hg19UCSC Ensembl
Outerchr7:4372595..4641802hg19UCSC Ensembl
Innerchr7:4443538..4584676hg18UCSC Ensembl
Outerchr7:4339121..4608328hg18UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38269208
hg19269208
hg18269208
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25782595, essv25790912
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3891022
Frequency
Sample Size3017
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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