A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512172



Internal ID20885503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:8431875..8432440hg38UCSC Ensembl
chr16:8481877..8482442hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38566
hg19566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18032980
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512172
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