A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17039363



Internal ID93965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119859324..119859550hg38UCSC Ensembl
chr10:121618836..121619062hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5508456
Supporting Variants
Samples
Known GenesMCMBP
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17039363
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.000624


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