A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6503268



Internal ID20876521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:17051401..17057300hg38UCSC Ensembl
Cytoband
Allele length
AssemblyAllele length
hg385900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2371n223
Supporting Variantsnssv18192576
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6503268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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