A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625052



Internal ID6665205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133534531..133564756hg38UCSC Ensembl
chr10:135348035..135378260hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3830226
hg1930226
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13984788, essv13984789, essv13984790
SamplesHG03882, HG03445, HG02075
Known GenesCYP2E1, SYCE1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625052
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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