A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207922



Internal ID20774962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:120231497..120248691hg38UCSC Ensembl
chr3:119950344..119967538hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3817195
hg1917195
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6373315
Supporting Variants
Samples
Known GenesGPR156
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207922
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