A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5603295



Internal ID8839243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:3923028..3931049hg38UCSC Ensembl
Outerchr16:3922871..3931202hg38UCSC Ensembl
Innerchr16:3973029..3981050hg19UCSC Ensembl
Outerchr16:3972872..3981203hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg388332
hg198332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2663437
Supporting Variants
SamplesHG00276
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5603295
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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