A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16897453



Internal ID172455
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15618125..15620538hg38UCSC Ensembl
chr1:15944620..15947033hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg382414
hg192414
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5422991
Supporting Variants
Samples
Known GenesDDI2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16897453
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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