A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6083245



Internal ID21992478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:75518497..75518497hg38UCSC Ensembl
chr15:75810838..75810838hg19UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17603137
Samples
Known GenesPTPN9
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6083245
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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