A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210124



Internal ID20777164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:84964033..84977061hg38UCSC Ensembl
chr3:85013184..85026212hg19UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3813029
hg1913029
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6369208
Supporting Variants
Samples
Known GenesCADM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210124
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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