A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17385237



Internal ID22443107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:65229184..65234706hg38UCSC Ensembl
chr18:62896420..62901942hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg385523
hg195523
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5931034
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17385237
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