A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18052320



Internal ID20619360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:152135945..152136313hg38UCSC Ensembl
chr1:152108421..152108789hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38369
hg19369
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6320140
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18052320
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00057


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