A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890896



Internal ID168109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156383511..156383762hg38UCSC Ensembl
chr1:156353302..156353553hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg38252
hg19252
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5431605
Supporting Variants
Samples
Known GenesRHBG
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890896
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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