A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6506469



Internal ID20879749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:23163301..23222900hg38UCSC Ensembl
chr15:22650168..22709666hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3859600
hg1959499
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2387n223
Supporting Variantsnssv18191419
Samples
Known GenesGOLGA8DP, MIR4509-1, MIR4509-2, MIR4509-3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6506469
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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