A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13894398



Internal ID5758434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91164679..91174151hg38UCSC Ensembl
Innerchr10:91164679..91174151hg38UCSC Ensembl
Outerchr10:91164591..91174258hg38UCSC Ensembl
chr10:92924436..92933908hg19UCSC Ensembl
Innerchr10:92924436..92933908hg19UCSC Ensembl
Outerchr10:92924348..92934015hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg389473
hg199473
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624200
Supporting Variants
SamplesNA19130
Known GenesPCGF5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13894398
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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