A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16892875



Internal ID169419
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:184410595..184415767hg38UCSC Ensembl
chr1:184379729..184384901hg19UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg385173
hg195173
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5446680
Supporting Variants
Samples
Known GenesC1orf21
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16892875
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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