A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13984504



Internal ID658689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133082541..133084963hg38UCSC Ensembl
Innerchr10:133082541..133084963hg38UCSC Ensembl
Outerchr10:133082398..133085072hg38UCSC Ensembl
chr10:134896045..134898467hg19UCSC Ensembl
Innerchr10:134896045..134898467hg19UCSC Ensembl
Outerchr10:134895902..134898576hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg382423
hg192423
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625027
Supporting Variants
SamplesHG00306
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13984504
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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