A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18101500



Internal ID20668540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:64430407..64432305hg38UCSC Ensembl
chr3:64416083..64417981hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg381899
hg191899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359232
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18101500
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