A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506669



Internal ID20879953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:63391801..63392500hg38UCSC Ensembl
chr16:63425705..63426404hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38700
hg19700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18031182
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506669
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