A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267383



Internal ID20476601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:50327363..50327363hg38UCSC Ensembl
chr20:48943900..48943900hg19UCSC Ensembl
Cytoband20q13.13
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4751437
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267383
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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