A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17488329



Internal ID22546246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16842528..16853893hg38UCSC Ensembl
chr2:17023795..17035160hg19UCSC Ensembl
Cytoband2p24.2
Allele length
AssemblyAllele length
hg3811366
hg1911366
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5831929
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17488329
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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