A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5521871



Internal ID298151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65337347..65337417hg38UCSC Ensembl
chr15:65629685..65629755hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704271
Samples
Known GenesIGDCC3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5521871
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