A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635394



Internal ID7022193
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94949356..94952521hg38UCSC Ensembl
chr14:95415693..95418858hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg383166
hg193166
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15103356, essv15103359, essv15103357, essv15103360, essv15103358, essv15103361
SamplesNA20878, HG04076, HG02595, HG02733, HG03868, HG00336
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635394
Frequency
Sample Size2504
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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