A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16890953



Internal ID168146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:157136009..157136173hg38UCSC Ensembl
chr1:157105801..157105965hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38165
hg19165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5418489
Supporting Variants
Samples
Known GenesETV3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16890953
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