A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16895321



Internal ID171059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:13910226..13917560hg38UCSC Ensembl
chr1:14236721..14244055hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg387335
hg197335
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431509
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16895321
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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