A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6514087



Internal ID20887438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:52049613..52087694hg38UCSC Ensembl
chr15:52341810..52379891hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3838082
hg1938082
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18187549
Samples
Known GenesMAPK6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6514087
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