A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277819



Internal ID20487037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:16177924..16177924hg38UCSC Ensembl
chr20:16158569..16158569hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38334
hg19334
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4765535
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277819
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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