A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16281178



Internal ID20490396
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:172627810..172627810hg38UCSC Ensembl
chr5:172054813..172054813hg19UCSC Ensembl
Cytoband5q35.1
Allele length
AssemblyAllele length
hg38454
hg19454
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758454
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16281178
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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