A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504079



Internal ID20877338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24202186..24509830hg38UCSC Ensembl
chr15:24447333..24754977hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38307645
hg19307645
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2406n223
Supporting Variantsnssv18187520
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504079
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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