A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2659032



Internal ID9925137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:8093536..8093918hg38UCSC Ensembl
Outerchr17:8093379..8094071hg38UCSC Ensembl
Innerchr17:7996854..7997236hg19UCSC Ensembl
Outerchr17:7996697..7997389hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38693
hg19693
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv532e199
Supporting Variantsessv5524349, essv6189404, essv5477734, essv5731515, essv6118674, essv5459466, essv6364615, essv6436342, essv6372811, essv6584436, essv6067246, essv6023027, essv6487141, essv5881902, essv5903466, essv6116857, essv6475597
SamplesNA18502, NA11995, NA12155, NA18967, NA19448, NA19313, NA19445, NA19462, NA19114, NA18853, NA18974, NA19434, NA19331, NA19334, NA19428, NA19376, NA12776
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2659032
Frequency
Sample Size1151
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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