A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13919364



Internal ID3171365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:105339955..105492496hg38UCSC Ensembl
chr10:107099713..107252254hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38152542
hg19152542
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624443
Supporting Variants
SamplesHG02789
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13919364
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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