A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16898356



Internal ID173047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15985382..16003597hg38UCSC Ensembl
chr1:16311877..16330092hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3818216
hg1918216
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5423130
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16898356
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000156


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