A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2661062



Internal ID9927167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:61764128..61764281hg38UCSC Ensembl
chr8:62676687..62676840hg19UCSC Ensembl
Cytoband8q12.3
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5607435, essv5908442, essv6401079, essv5644863, essv6242181, essv6305617, essv5717582, essv5566152, essv5873596, essv6033031, essv5888282, essv6077281, essv6264756, essv5597388, essv5954628, essv5696657, essv5810492
SamplesNA18861, NA19092, NA20332, NA18870, NA20317, NA19461, NA19453, NA18912, NA19452, NA19375, NA19440, NA19331, NA19428, NA19468, NA19430, NA19129, NA18511
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2661062
Frequency
Sample Size1151
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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