A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17522411



Internal ID21846770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:199675291..199675291hg38UCSC Ensembl
chr1:199644419..199644419hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38272
hg19272
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043090
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17522411
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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