A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13902015



Internal ID962766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:94179058..94184515hg38UCSC Ensembl
Innerchr10:94179558..94184015hg38UCSC Ensembl
Outerchr10:94178058..94185515hg38UCSC Ensembl
chr10:95938815..95944272hg19UCSC Ensembl
Innerchr10:95939315..95943772hg19UCSC Ensembl
Outerchr10:95937815..95945272hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg385458
hg195458
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624248
Supporting Variants
SamplesHG00593
Known GenesPLCE1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13902015
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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