A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9753152



Internal ID18727398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:39592728..39594458hg38UCSC Ensembl
Outerchr17:39592680..39594623hg38UCSC Ensembl
Innerchr17:37748981..37750711hg19UCSC Ensembl
Outerchr17:37748933..37750876hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg381944
hg191944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3554405
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9753152
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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