A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657951



Internal ID9924056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:17034549..17038452hg38UCSC Ensembl
Outerchr4:17034392..17038605hg38UCSC Ensembl
Innerchr4:17036172..17040075hg19UCSC Ensembl
Outerchr4:17036015..17040228hg19UCSC Ensembl
Cytoband4p15.32
Allele length
AssemblyAllele length
hg384214
hg194214
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5907178, essv5607262, essv5542768
SamplesNA19247, NA19108, NA19102
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657951
Frequency
Sample Size1151
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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