A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624043



Internal ID7010899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:84760778..84776356hg38UCSC Ensembl
Innerchr10:84760778..84776356hg38UCSC Ensembl
Outerchr10:84760278..84776856hg38UCSC Ensembl
chr10:86520534..86536112hg19UCSC Ensembl
Innerchr10:86520534..86536112hg19UCSC Ensembl
Outerchr10:86520034..86536612hg19UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3815579
hg1915579
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13882135, essv13882133, essv13882134
SamplesNA18574, HG03624, NA20876
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624043
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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