A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624230



Internal ID7011086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:92864611..92873535hg38UCSC Ensembl
Innerchr10:92864611..92873535hg38UCSC Ensembl
Outerchr10:92864341..92873968hg38UCSC Ensembl
chr10:94624368..94633292hg19UCSC Ensembl
Innerchr10:94624368..94633292hg19UCSC Ensembl
Outerchr10:94624098..94633725hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg388925
hg198925
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13899207, essv13899196, essv13899209, essv13899199, essv13899200, essv13899213, essv13899206, essv13899214, essv13899202, essv13899205, essv13899198, essv13899211, essv13899204, essv13899212, essv13899215, essv13899208, essv13899197, essv13899210, essv13899203, essv13899201
SamplesHG03773, NA20891, HG04002, HG04038, HG03796, NA20900, HG03873, HG04106, HG03696, HG04035, HG03752, HG04159, HG03866, NA20870, NA19467, HG03846, NA21125, HG03729, HG04023, HG03998
Known GenesEXOC6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624230
Frequency
Sample Size2504
Observed Gain0
Observed Loss20
Observed Complex0
Frequencyn/a


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