A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17482661



Internal ID22540567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218174423..218179710hg38UCSC Ensembl
chr2:219039146..219044433hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg385288
hg195288
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5832207
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17482661
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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