A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640941



Internal ID21832988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:40620347..40620347hg38UCSC Ensembl
chr21:41992273..41992273hg19UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg38212
hg19212
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6102805
Supporting Variants
Samples
Known GenesDSCAM, DSCAM-IT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640941
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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