A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15359755



Internal ID5361571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1356693..1364925hg38UCSC Ensembl
chr16:1406694..1414926hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg388233
hg198233
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3637615
Supporting Variants
SamplesHG03511
Known GenesGNPTG, UNKL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15359755
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