A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17485632



Internal ID22543543
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146590476..146599956hg38UCSC Ensembl
chr3:146308263..146317743hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg389481
hg199481
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5834356
Supporting Variants
Samples
Known GenesPLSCR5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17485632
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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