A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622514



Internal ID7009373
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18710624..18716437hg38UCSC Ensembl
Innerchr10:18710627..18716435hg38UCSC Ensembl
Outerchr10:18710622..18716440hg38UCSC Ensembl
chr10:18999553..19005366hg19UCSC Ensembl
Innerchr10:18999556..19005364hg19UCSC Ensembl
Outerchr10:18999551..19005369hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg385814
hg195814
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13710226, essv13710229, essv13710230, essv13710228, essv13710227
SamplesHG02375, HG02390, NA18572, HG00844, HG02186
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622514
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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