A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13914614



Internal ID6286633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103392636..103459758hg38UCSC Ensembl
chr10:105152393..105219515hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3867123
hg1967123
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624413
Supporting Variants
SamplesNA19819
Known GenesCALHM1, CALHM2, MIR1307, PDCD11, USMG5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13914614
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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