A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624699



Internal ID7011549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119180133..119184614hg38UCSC Ensembl
Innerchr10:119180145..119184602hg38UCSC Ensembl
Outerchr10:119180121..119184626hg38UCSC Ensembl
chr10:120939645..120944126hg19UCSC Ensembl
Innerchr10:120939657..120944114hg19UCSC Ensembl
Outerchr10:120939633..120944138hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg384482
hg194482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13946774, essv13946777, essv13946776, essv13946775, essv13946773
SamplesHG04038, HG03736, HG04107, HG03824, HG03672
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624699
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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