A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17640031



Internal ID21832078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:43743211..43743211hg38UCSC Ensembl
chr21:45163092..45163092hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg38269
hg19269
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6105570
Supporting Variants
Samples
Known GenesPDXK
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17640031
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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