A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623051



Internal ID6663219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43887894..43888636hg38UCSC Ensembl
Innerchr10:43887895..43888635hg38UCSC Ensembl
Outerchr10:43887893..43888637hg38UCSC Ensembl
chr10:44383342..44384084hg19UCSC Ensembl
Innerchr10:44383343..44384083hg19UCSC Ensembl
Outerchr10:44383341..44384085hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38743
hg19743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13764547, essv13764545, essv13764531, essv13764546, essv13764543, essv13764542, essv13764534, essv13764535, essv13764548, essv13764540, essv13764537, essv13764532, essv13764541, essv13764549, essv13764544, essv13764539, essv13764538, essv13764536, essv13764533, essv13764550
SamplesNA18870, HG01359, NA18874, HG02549, HG02322, NA19355, NA19383, NA19239, NA18856, NA06986, HG02439, HG01889, HG01697, NA19201, HG01626, HG03139, HG02476, HG03117, HG02555, HG02860
Known GenesLINC00840
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623051
Frequency
Sample Size2504
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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