A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485728



Internal ID22543640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15347311..15353138hg38UCSC Ensembl
chr3:15388818..15394645hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg385828
hg195828
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5835000
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485728
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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