A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502834



Internal ID20876082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:9553032..9556164hg38UCSC Ensembl
chr16:9646889..9650021hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg383133
hg193133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18033953
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502834
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