A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17517602



Internal ID21841961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:158218698..158218698hg38UCSC Ensembl
chr1:158188488..158188488hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg382224
hg192224
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6054428
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17517602
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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