A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6504858



Internal ID20878122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:17036801..17044700hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg387900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2366n223
Supporting Variantsnssv18183062
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6504858
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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