A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17492569



Internal ID22550496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47532860..47568954hg38UCSC Ensembl
chr3:47574350..47610444hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg3836095
hg1936095
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5836304
Supporting Variants
Samples
Known GenesCSPG5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17492569
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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