A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15362420



Internal ID5364236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2162205..2163028hg38UCSC Ensembl
Innerchr16:2162207..2163027hg38UCSC Ensembl
Outerchr16:2162204..2163030hg38UCSC Ensembl
chr16:2212206..2213029hg19UCSC Ensembl
Innerchr16:2212208..2213028hg19UCSC Ensembl
Outerchr16:2212205..2213031hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38824
hg19824
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637629
Supporting Variants
SamplesHG00323
Known GenesTRAF7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15362420
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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