A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15385613



Internal ID5387429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:15415766..15522718hg38UCSC Ensembl
chr16:15509623..15616575hg19UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg38106953
hg19106953
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638032
Supporting Variants
SamplesHG03072
Known GenesC16orf45
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15385613
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