A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13914615



Internal ID6286629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:103412843..103459270hg38UCSC Ensembl
chr10:105172600..105219027hg19UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3846428
hg1946428
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624414
Supporting Variants
SamplesNA19819
Known GenesCALHM1, CALHM2, PDCD11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13914615
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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