A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503436



Internal ID20876691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:50771720..50775310hg38UCSC Ensembl
chr16:50805631..50809221hg19UCSC Ensembl
Cytoband16q12.1
Allele length
AssemblyAllele length
hg383591
hg193591
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18030028
Samples
Known GenesCYLD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503436
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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