A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17532516



Internal ID21856872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:223478920..223479342hg38UCSC Ensembl
chr1:223652262..223652684hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg38423
hg19423
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5982720
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17532516
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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