A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18059197



Internal ID20626237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:228238001..228240100hg38UCSC Ensembl
chr1:228425702..228427801hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6329051
Supporting Variants
Samples
Known GenesOBSCN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18059197
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