A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624316



Internal ID7011172
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:97560913..97561771hg38UCSC Ensembl
Innerchr10:97560916..97561769hg38UCSC Ensembl
Outerchr10:97560911..97561774hg38UCSC Ensembl
chr10:99320670..99321528hg19UCSC Ensembl
Innerchr10:99320673..99321526hg19UCSC Ensembl
Outerchr10:99320668..99321531hg19UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38859
hg19859
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13908174, essv13908170, essv13908171, essv13908172, essv13908173
SamplesHG01412, NA20863, HG00243, HG00106, NA21086
Known GenesUBTD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624316
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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