A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6515268



Internal ID20888627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:55820593..55829396hg38UCSC Ensembl
chr15:56112791..56121594hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg388804
hg198804
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18189779
Samples
Known GenesNEDD4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6515268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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