A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665260



Internal ID9931365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:62168366..62174633hg38UCSC Ensembl
chr15:62460565..62466832hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg386268
hg196268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6462642, essv6184191, essv6536898, essv6259774
SamplesHG01167, NA19471, NA18853, NA19213
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665260
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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