A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16259470



Internal ID20468688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:44288423..44288489hg38UCSC Ensembl
chr15:44580621..44580687hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg3867
hg1967
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4747365
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16259470
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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