A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029162



Internal ID20596202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:30460101..30467700hg38UCSC Ensembl
chr16:30471422..30479021hg19UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg387600
hg197600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6512190
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029162
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer