A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672262



Internal ID9938367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:62663408..62664798hg38UCSC Ensembl
Outerchr15:62663251..62664951hg38UCSC Ensembl
Innerchr15:62955607..62956997hg19UCSC Ensembl
Outerchr15:62955450..62957150hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6012698, essv6555844, essv5738937, essv6324078, essv6461848, essv6142543, essv6308902, essv6093333, essv5919697, essv5554023, essv5860373, essv6224812, essv5997971, essv5844859, essv6510966, essv5413211
SamplesNA18980, NA18486, NA18545, NA19190, NA19005, NA18940, NA19131, NA18942, NA19210, NA18856, NA18853, NA19452, NA19093, NA18552, NA19129, NA18522
Known GenesTLN2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672262
Frequency
Sample Size1151
Observed Gain0
Observed Loss16
Observed Complex0
Frequencyn/a


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