A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485476



Internal ID22543387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:41984671..41985979hg38UCSC Ensembl
chr2:42211811..42213119hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg381309
hg191309
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832663
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485476
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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