A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9764224



Internal ID18738470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7907472..7907845hg38UCSC Ensembl
Outerchr5:7907444..7907939hg38UCSC Ensembl
Innerchr5:7907585..7907958hg19UCSC Ensembl
Outerchr5:7907557..7908052hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38496
hg19496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3565477
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9764224
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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