A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17521910



Internal ID21846269
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:162720490..162720490hg38UCSC Ensembl
chr1:162690280..162690280hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg382120
hg192120
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6045803
Supporting Variants
Samples
Known GenesDDR2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17521910
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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