A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625008



Internal ID7011853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:132820048..132833523hg38UCSC Ensembl
chr10:134633552..134647027hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3813476
hg1913476
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13983507, essv13983510, essv13983508, essv13983504, essv13983512, essv13983503, essv13983505, essv13983513, essv13983506, essv13983502, essv13983511, essv13983509
SamplesNA20802, NA18625, NA20769, HG01110, NA20775, NA20757, NA20800, NA20760, NA20581, NA19078, NA18631, NA19431
Known GenesTTC40
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625008
Frequency
Sample Size2504
Observed Gain12
Observed Loss0
Observed Complex0
Frequencyn/a


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