A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6500796



Internal ID20874024
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:3055397..3075186hg38UCSC Ensembl
chr16:3105398..3125187hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg3819790
hg1919790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18029166
Samples
Known GenesIL32, MMP25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6500796
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