A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13984608



Internal ID3986424
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3625046
Supporting Variants
SamplesHG03445
Known GenesCYP2E1, SCART1, SYCE1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13984608
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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