A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16284532



Internal ID20493750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:24509203..24509271hg38UCSC Ensembl
chr16:24520524..24520592hg19UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4732669
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16284532
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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