A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262140



Internal ID20471358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:53935648..53935648hg38UCSC Ensembl
chr20:52552187..52552187hg19UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg3875
hg1975
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753754
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262140
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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