A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17490666



Internal ID22548590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31524891..31530165hg38UCSC Ensembl
chr3:31566383..31571657hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg385275
hg195275
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835911
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17490666
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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