A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623771



Internal ID7010627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71114942..71119587hg38UCSC Ensembl
Innerchr10:71114992..71119537hg38UCSC Ensembl
Outerchr10:71114892..71119637hg38UCSC Ensembl
chr10:72874699..72879344hg19UCSC Ensembl
Innerchr10:72874749..72879294hg19UCSC Ensembl
Outerchr10:72874649..72879394hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg384646
hg194646
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13859463
SamplesNA20905
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623771
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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