A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18191419



Internal ID20758459
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 StatusS
Merged Variantsnsv6506469
Supporting Variants
Samples
Known GenesGOLGA8DP, MIR4509-1, MIR4509-2, MIR4509-3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18191419
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.03983


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