A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3635637



Internal ID7022436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:105079623..105114221hg38UCSC Ensembl
chr14:105545960..105580558hg19UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3834599
hg1934599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15117402
SamplesHG00105
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3635637
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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