A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16901432



Internal ID1764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:36333346..36336703hg38UCSC Ensembl
chr1:36798947..36802304hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg383358
hg193358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5420531
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16901432
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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