A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890528



Internal ID167859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149145440..149168587hg38UCSC Ensembl
chr1:144528402..144551537hg19UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg3823148
hg1923136
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431913
Supporting Variants
Samples
Known GenesLOC100288142
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890528
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.030732


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer