A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3542756



Internal ID18743832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:156165020..156165915hg38UCSC Ensembl
Outerchr7:156165018..156165920hg38UCSC Ensembl
Innerchr7:155957714..155958609hg19UCSC Ensembl
Outerchr7:155957712..155958614hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38903
hg19903
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9741503
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3542756
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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