A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17639214



Internal ID21831261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:41249257..41249257hg38UCSC Ensembl
chr21:42621184..42621184hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3889
hg1989
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6107042
Supporting Variants
Samples
Known GenesBACE2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17639214
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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