A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18029130



Internal ID20596170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2993686..2994234hg38UCSC Ensembl
chr16:3043687..3044235hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38549
hg19549
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6504342
Supporting Variants
Samples
Known GenesLINC00514
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18029130
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