A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062339



Internal ID20629379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:63872292..63872876hg38UCSC Ensembl
chr1:64337963..64338547hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38585
hg19585
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6327921
Supporting Variants
Samples
Known GenesROR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062339
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00029


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