A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3542752



Internal ID18743828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156126606..156127039hg38UCSC Ensembl
Outerchr7:156126592..156127110hg38UCSC Ensembl
Innerchr7:155919300..155919733hg19UCSC Ensembl
Outerchr7:155919286..155919804hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38519
hg19519
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9741499
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3542752
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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