A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18210375



Internal ID20777415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158349855..158363421hg38UCSC Ensembl
chr3:158067644..158081210hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3813567
hg1913567
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6372421
Supporting Variants
Samples
Known GenesRSRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18210375
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