A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3540987



Internal ID18742063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:434582..434710hg38UCSC Ensembl
Outerchr7:434571..434726hg38UCSC Ensembl
Innerchr7:474565..474693hg19UCSC Ensembl
Outerchr7:474554..474709hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9739734
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3540987
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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