A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661720



Internal ID9927825
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:59488934..59489428hg38UCSC Ensembl
chr8:60401493..60401987hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38495
hg19495
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5874185, essv6176968, essv5448842, essv6208224
SamplesNA19684, HG01134, HG00254, NA07051
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661720
Frequency
Sample Size1151
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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