A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15040399



Internal ID3400588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:63590104..63619709hg38UCSC Ensembl
chr14:64056822..64086427hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3829606
hg1929606
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3634734
Supporting Variants
SamplesHG03048
Known GenesWDR89
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15040399
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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