A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890923



Internal ID168127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156764307..156765226hg38UCSC Ensembl
chr1:156734099..156735018hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38920
hg19920
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5433131
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890923
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000312


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