A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16266594



Internal ID20475812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:31564142..31564142hg38UCSC Ensembl
chr21:32936455..32936455hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767382
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16266594
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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