A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17034049



Internal ID90399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63272540..63423094hg38UCSC Ensembl
chr10:65032300..65182854hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38150555
hg19150555
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5493656
Supporting Variants
Samples
Known GenesJMJD1C, MIR1296
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17034049
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