A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9740655



Internal ID18368215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:74369856..74370104hg38UCSC Ensembl
Outerchr7:74369802..74370155hg38UCSC Ensembl
Innerchr7:73784186..73784434hg19UCSC Ensembl
Outerchr7:73784132..73784485hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3541908
Supporting Variants
Samples
Known GenesCLIP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9740655
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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