A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622935



Internal ID7009793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:36766142..36770532hg38UCSC Ensembl
chr10:37055070..37059460hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg384391
hg194391
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13756691, essv13756689, essv13756690, essv13756688
SamplesHG03765, HG02697, HG01589, HG01894
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622935
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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