A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17638611



Internal ID21830658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43063078..43063078hg38UCSC Ensembl
chr21:44483188..44483188hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6103938
Supporting Variants
Samples
Known GenesCBS
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17638611
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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