A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17473629



Internal ID22531522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74828365..74829704hg38UCSC Ensembl
chr15:75120706..75122045hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg381340
hg191340
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861145
Supporting Variants
Samples
Known GenesCPLX3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17473629
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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