A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3554396



Internal ID18408786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:38819263..38819418hg38UCSC Ensembl
Outerchr17:38819247..38819430hg38UCSC Ensembl
Innerchr17:36975516..36975671hg19UCSC Ensembl
Outerchr17:36975500..36975683hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9753143
Samples
Known GenesCWC25
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3554396
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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