A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6496907



Internal ID20870110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:75924898..75997761hg38UCSC Ensembl
chr16:75958796..76031659hg19UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3872864
hg1972864
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2936n223
Supporting Variantsnssv18032755
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6496907
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