A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623158



Internal ID6663326
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48761141..48769233hg38UCSC Ensembl
Innerchr10:48761141..48769233hg38UCSC Ensembl
Outerchr10:48761083..48769326hg38UCSC Ensembl
chr10:49969186..49977278hg19UCSC Ensembl
Innerchr10:49969186..49977278hg19UCSC Ensembl
Outerchr10:49969128..49977371hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg388093
hg198093
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13796099
SamplesNA20760
Known GenesWDFY4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623158
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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