A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639823



Internal ID7026601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5868212..5887059hg38UCSC Ensembl
Innerchr17:5868712..5886559hg38UCSC Ensembl
Outerchr17:5867212..5888059hg38UCSC Ensembl
chr17:5771532..5790379hg19UCSC Ensembl
Innerchr17:5772032..5789879hg19UCSC Ensembl
Outerchr17:5770532..5791379hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3818848
hg1918848
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv558e214
Supporting Variantsessv15601062, essv15601061
SamplesNA20533, HG03919
Known GenesLOC339166
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639823
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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