A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17623344



Internal ID21815391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:38653044..38653044hg38UCSC Ensembl
chr20:37281687..37281687hg19UCSC Ensembl
Cytoband20q11.23
Allele length
AssemblyAllele length
hg38104
hg19104
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6112037
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17623344
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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