A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6511368



Internal ID20884695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23195601..23226600hg38UCSC Ensembl
chr15:22646468..22677467hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3831000
hg1931000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18178961
Samples
Known GenesMIR4509-1, MIR4509-2, MIR4509-3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6511368
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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