A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15569863



Internal ID3089889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:89813127..89823660hg38UCSC Ensembl
chr16:89879535..89890068hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3810534
hg1910534
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639599
Supporting Variants
SamplesHG02716
Known GenesFANCA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15569863
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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