A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498238



Internal ID20871446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72246224..72248464hg38UCSC Ensembl
chr15:72538565..72540805hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg382241
hg192241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18179609
Samples
Known GenesPARP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498238
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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