A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16891097



Internal ID168241
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:149656000..149664293hg38UCSC Ensembl
chr1:149627610..149635895hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg388294
hg198286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138499
Supporting Variants
Samples
Known GenesLINC00869
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16891097
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.107421


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