A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3642840



Internal ID7029609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:65637666..65638492hg38UCSC Ensembl
Innerchr18:65637668..65638490hg38UCSC Ensembl
Outerchr18:65637664..65638494hg38UCSC Ensembl
chr18:63304902..63305728hg19UCSC Ensembl
Innerchr18:63304904..63305726hg19UCSC Ensembl
Outerchr18:63304900..63305730hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38827
hg19827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15909891, essv15909908, essv15909901, essv15909921, essv15909894, essv15909913, essv15909915, essv15909900, essv15909909, essv15909905, essv15909922, essv15909916, essv15909887, essv15909893, essv15909896, essv15909895, essv15909919, essv15909907, essv15909898, essv15909889, essv15909918, essv15909902, essv15909917, essv15909903, essv15909890, essv15909904, essv15909920, essv15909923, essv15909897, essv15909892, essv15909899, essv15909886, essv15909910, essv15909906, essv15909911, essv15909912, essv15909914, essv15909888
SamplesHG00626, HG01413, HG00592, NA18947, HG01326, NA18639, HG01686, HG01944, NA21128, HG03808, NA18942, HG00610, NA19088, HG03917, HG02489, HG01849, HG02402, NA18613, HG00982, HG00732, NA18956, HG01852, HG01447, NA18566, HG00690, NA12249, HG03571, HG02586, HG00410, NA18953, HG02049, HG01375, HG01489, NA20348, NA19060, HG02116, NA18957, NA18968
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3642840
Frequency
Sample Size2504
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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