A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508158



Internal ID20881456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30163207..30172803hg38UCSC Ensembl
chr16:30174528..30184124hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg389597
hg199597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029150
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508158
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