A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13899207



Internal ID4539704
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624230
Supporting Variants
SamplesHG04035
Known GenesEXOC6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13899207
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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