A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6508302



Internal ID20881601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43385667..43393682hg38UCSC Ensembl
chr15:43677865..43685880hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg388016
hg198016
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18192455
Samples
Known GenesRNU6-28P, TUBGCP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6508302
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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