A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497117



Internal ID20870321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:50148901..50192900hg38UCSC Ensembl
chr15:50441098..50485097hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg3844000
hg1944000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2534n223
Supporting Variantsnssv18181826
Samples
Known GenesSLC27A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497117
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