A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18062144



Internal ID20629184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:61557916..61562890hg38UCSC Ensembl
chr1:62023588..62028562hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg384975
hg194975
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317740
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18062144
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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