A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517743



Internal ID21842102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151483102..151489274hg38UCSC Ensembl
chr1:151455578..151461750hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg386173
hg196173
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981442
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17517743
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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