A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661482



Internal ID9927587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64705513..64715500hg38UCSC Ensembl
chr15:64997712..65007699hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg389988
hg199988
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6577140, essv6161083, essv5632168, essv5887949, essv6329218
SamplesHG01140, NA20287, NA18856, NA19225, NA19834
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661482
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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