A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17054428



Internal ID104120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17022272..17027230hg38UCSC Ensembl
chr12:17175206..17180164hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg384959
hg194959
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5496985
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17054428
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001874


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