A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16280713



Internal ID20489931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40050450..40051891hg38UCSC Ensembl
chr15:40342651..40344092hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381442
hg191442
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4742923
Supporting Variants
Samples
Known GenesSRP14-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16280713
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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