A curated catalogue of human genomic structural variation




Variant Details

Variant: essv14890449



Internal ID4892265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:107071569..107169184hg38UCSC Ensembl
chr13:107723917..107821532hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg3897616
hg1997616
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3633482
Supporting Variants
SamplesHG00257
Known GenesFAM155A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv14890449
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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