A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636098



Internal ID7022894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:33982700..33986813hg38UCSC Ensembl
Innerchr15:33982701..33986812hg38UCSC Ensembl
Outerchr15:33982699..33986814hg38UCSC Ensembl
chr15:34274901..34279014hg19UCSC Ensembl
Innerchr15:34274902..34279013hg19UCSC Ensembl
Outerchr15:34274900..34279015hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg384114
hg194114
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15210412, essv15210416, essv15210402, essv15210419, essv15210403, essv15210396, essv15210409, essv15210397, essv15210420, essv15210395, essv15210406, essv15210400, essv15210410, essv15210404, essv15210415, essv15210414, essv15210398, essv15210417, essv15210413, essv15210401, essv15210399, essv15210411, essv15210421, essv15210408, essv15210422, essv15210407, essv15210405, essv15210418
SamplesNA20877, HG02727, NA20864, HG03235, HG02733, NA21109, NA20889, NA21106, HG02793, HG03718, NA20885, NA20521, HG04195, HG02731, HG01880, HG03919, HG03742, NA20867, NA20866, NA21086, HG02649, HG03672, HG04118, HG04239, NA20897, NA20847, HG03998, HG03882
Known GenesAVEN, CHRM5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636098
Frequency
Sample Size2504
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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