A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890629



Internal ID167933
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153784587..153791000hg38UCSC Ensembl
chr1:153757063..153763476hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg386414
hg196414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138256
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890629
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000473


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