A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511196



Internal ID20884522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:84653777..84656525hg38UCSC Ensembl
chr16:84687383..84690131hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg382749
hg192749
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033039
Samples
Known GenesKLHL36
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511196
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