A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3625046



Internal ID6665199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:133442774..133554993hg38UCSC Ensembl
chr10:135256278..135368497hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38112220
hg19112220
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13984608
SamplesHG03445
Known GenesCYP2E1, SCART1, SYCE1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3625046
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer