A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17526999



Internal ID21851356
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156375372..156376661hg38UCSC Ensembl
chr1:156345163..156346452hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg381290
hg191290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981404
Supporting Variants
Samples
Known GenesRHBG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17526999
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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