A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17525057



Internal ID21849415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:168879782..168879782hg38UCSC Ensembl
chr1:168849020..168849020hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6050229
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17525057
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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