A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2672052



Internal ID9938157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:24268804..24269641hg38UCSC Ensembl
chr20:24249440..24250277hg19UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg38838
hg19838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6099392, essv5653598, essv5420960, essv5860515, essv5511481, essv5869055, essv5571551, essv6057673, essv5703831, essv6115502, essv6185198, essv6144806, essv5992630, essv5454962, essv6538918, essv5910668, essv6128492, essv6509545, essv6459633, essv6225950
SamplesNA19701, NA19332, NA19704, HG01188, NA19396, NA20287, NA19904, NA19384, NA19471, HG00740, NA19452, NA19318, NA19625, NA19436, NA19401, NA19835, NA19818, NA19713, NA19474, NA19429
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2672052
Frequency
Sample Size1151
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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