A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17404884



Internal ID22462754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:89956731..89956797hg38UCSC Ensembl
chr1:90422290..90422356hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5878818
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17404884
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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