A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497019



Internal ID20870222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30804151..30807663hg38UCSC Ensembl
chr16:30815472..30818984hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg383513
hg193513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497019
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