A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18103166



Internal ID20670206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:81621401..81623200hg38UCSC Ensembl
chr3:81670552..81672351hg19UCSC Ensembl
Cytoband3p12.2
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6357252
Supporting Variants
Samples
Known GenesGBE1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18103166
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