A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3631408



Internal ID6671535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:19860755..19874758hg38UCSC Ensembl
chr13:20434895..20448898hg19UCSC Ensembl
Cytoband13q12.11
Allele length
AssemblyAllele length
hg3814004
hg1914004
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv14657535, essv14657536, essv14657533, essv14657531, essv14657532, essv14657534, essv14657537
SamplesHG01326, NA12812, NA12761, NA19041, HG00732, HG01107, HG00353
Known GenesZMYM5
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3631408
Frequency
Sample Size2504
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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