A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18055143



Internal ID20622183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:189864657..189913318hg38UCSC Ensembl
chr1:189833787..189882448hg19UCSC Ensembl
Cytoband1q31.1
Allele length
AssemblyAllele length
hg3848662
hg1948662
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6332451
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18055143
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