A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2663636



Internal ID9929741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:103001939..103002285hg38UCSC Ensembl
chr8:104014167..104014513hg19UCSC Ensembl
Cytoband8q22.3
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6483461, essv6466953, essv5744322, essv6157063, essv6015594, essv5902943, essv5580468, essv5418782, essv5997309, essv5529169, essv6146173
SamplesHG01173, HG01374, NA19404, NA19385, NA19317, NA19239, HG01073, NA19240, NA19472, NA19468, NA19661
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2663636
Frequency
Sample Size1151
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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