A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636573



Internal ID7023367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55986870..56021506hg38UCSC Ensembl
chr15:56279068..56313704hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg3834637
hg1934637
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15256388, essv15256389
SamplesHG04214, HG04107
Known GenesNEDD4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636573
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer