A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17358956



Internal ID22584625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:22374434..22377552hg38UCSC Ensembl
chr1:22700927..22704045hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg383119
hg193119
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5875078
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17358956
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