A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3542628



Internal ID18743704
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149156633..149157275hg38UCSC Ensembl
Outerchr7:149156601..149157291hg38UCSC Ensembl
Innerchr7:148853725..148854367hg19UCSC Ensembl
Outerchr7:148853693..148854383hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38691
hg19691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9741375
Samples
Known GenesZNF398
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3542628
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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