A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17534226



Internal ID21858582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:171983398..171983398hg38UCSC Ensembl
chr1:171952538..171952538hg19UCSC Ensembl
Cytoband1q24.3
Allele length
AssemblyAllele length
hg38132
hg19132
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042316
Supporting Variants
Samples
Known GenesDNM3
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17534226
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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