A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624417



Internal ID7011273
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103504194..103506754hg38UCSC Ensembl
Innerchr10:103504194..103506754hg38UCSC Ensembl
Outerchr10:103503944..103507074hg38UCSC Ensembl
chr10:105263951..105266511hg19UCSC Ensembl
Innerchr10:105263951..105266511hg19UCSC Ensembl
Outerchr10:105263701..105266831hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg382561
hg192561
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13914623, essv13914624, essv13914627, essv13914628, essv13914626, essv13914620, essv13914622, essv13914619, essv13914621, essv13914625
SamplesNA21108, HG04033, HG03844, HG03785, HG03908, HG03786, HG03871, HG03846, HG03973, HG04080
Known GenesNEURL1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624417
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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