A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498015



Internal ID20871223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:67660801..67661200hg38UCSC Ensembl
chr16:67694704..67695103hg19UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031376
Samples
Known GenesACD, PARD6A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498015
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