A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102973



Internal ID20670013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58893527..58896431hg38UCSC Ensembl
chr3:58879253..58882157hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg382905
hg192905
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6368273
Supporting Variants
Samples
Known GenesC3orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102973
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