A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661170



Internal ID9927275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:17140617..17141053hg38UCSC Ensembl
Outerchr5:17140460..17141206hg38UCSC Ensembl
Innerchr5:17140726..17141162hg19UCSC Ensembl
Outerchr5:17140569..17141315hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg38747
hg19747
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6356359, essv6462773, essv6481975, essv6077921
SamplesNA19359, NA19462, NA19311, NA19429
Known GenesLOC285696
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661170
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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