A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640816



Internal ID7027590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:54235415..54236085hg38UCSC Ensembl
Innerchr17:54235444..54236056hg38UCSC Ensembl
Outerchr17:54235386..54236114hg38UCSC Ensembl
chr17:52312776..52313446hg19UCSC Ensembl
Innerchr17:52312805..52313417hg19UCSC Ensembl
Outerchr17:52312747..52313475hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg38671
hg19671
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15701743
SamplesNA19010
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640816
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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