A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17489169



Internal ID22547088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109616526..109621507hg38UCSC Ensembl
chr3:109335373..109340354hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg384982
hg194982
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834265
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17489169
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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