A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3633583



Internal ID7020392
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:112656199..112668144hg38UCSC Ensembl
chr13:113310513..113322458hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3811946
hg1911946
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14901138, essv14901137, essv14901139, essv14901136
SamplesHG00524, NA12813, NA12761, HG00234
Known GenesC13orf35
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3633583
Frequency
Sample Size2504
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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