A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2660864



Internal ID9926969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:61601789..61602045hg38UCSC Ensembl
Outerchr5:61601418..61602415hg38UCSC Ensembl
Innerchr5:60897616..60897872hg19UCSC Ensembl
Outerchr5:60897245..60898242hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg38998
hg19998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6187415, essv6153430, essv5990842, essv5834392, essv6427592, essv5698942, essv6136803, essv6276653, essv6094812, essv6375380, essv6156472, essv5677416, essv5691780, essv6413736, essv5738998, essv6598209, essv5447699, essv5496143, essv6332634, essv6446424, essv5688818, essv6340460, essv5860419, essv6420925, essv5412913, essv5779587, essv6205022, essv6309565, essv5698800
SamplesHG01441, HG01389, HG01374, HG01465, HG01456, HG01461, HG01140, HG01350, HG01351, HG01488, HG01492, HG01354, HG01365, HG01134, HG01440, HG01124, HG01353, HG01136, HG01384, HG01390, HG01148, HG01357, HG01375, HG01137, HG01489, HG01491, HG01377, HG01125, HG01437
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2660864
Frequency
Sample Size1151
Observed Gain0
Observed Loss29
Observed Complex0
Frequencyn/a


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