A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637960



Internal ID7024747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:12446954..12461749hg38UCSC Ensembl
chr16:12540811..12555606hg19UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3814796
hg1914796
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15377433
SamplesHG03902
Known GenesSNX29
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637960
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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