A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13696202



Internal ID3698018
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12069904..12082451hg38UCSC Ensembl
chr10:12111903..12124450hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3812548
hg1912548
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622357
Supporting Variants
SamplesHG03025
Known GenesDHTKD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13696202
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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