A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15362846



Internal ID5364662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3055679..3070944hg38UCSC Ensembl
chr16:3105680..3120945hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3815266
hg1915266
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637647
Supporting Variants
SamplesNA20585
Known GenesIL32, MMP25
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15362846
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