A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16907263



Internal ID5630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:71059432..71059491hg38UCSC Ensembl
chr1:71525115..71525174hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6138838
Supporting Variants
Samples
Known GenesZRANB2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16907263
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.005169


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