A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625027



Internal ID7011871
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 State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13984510, essv13984509, essv13984507, essv13984517, essv13984504, essv13984512, essv13984508, essv13984505, essv13984516, essv13984514, essv13984513, essv13984511, essv13984518, essv13984506, essv13984515
SamplesHG00306, NA18995, NA19038, NA20412, NA18954, NA18645, HG03785, NA18747, NA18939, NA19031, NA19309, NA12873, NA19117, NA18957, NA19146
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625027
Frequency
Sample Size2504
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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