A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17531703



Internal ID21856059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158473774..158473774hg38UCSC Ensembl
chr1:158443564..158443564hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38127
hg19127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6043265
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17531703
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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