A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5496760



Internal ID273828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:120591000..120711121hg38UCSC Ensembl
chr10:122350512..122470633hg19UCSC Ensembl
Cytoband10q26.12
Allele length
AssemblyAllele length
hg38120122
hg19120122
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17040337
Samples
Known GenesC10orf85, MIR5694
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5496760
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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