A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17472894



Internal ID22530786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:54254792..54255991hg38UCSC Ensembl
chr15:54546990..54548189hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5861346
Supporting Variants
Samples
Known GenesUNC13C
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17472894
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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