A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5490093



Internal ID267355
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:15845099..15845192hg38UCSC Ensembl
chr10:15887098..15887191hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17032131
Samples
Known GenesFAM188A
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5490093
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