A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639849



Internal ID21831896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:16398029..16398029hg38UCSC Ensembl
chr21:17770349..17770349hg19UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6101512
Supporting Variants
Samples
Known GenesLINC00478
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639849
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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