A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507154



Internal ID20880442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:57568521..57569176hg38UCSC Ensembl
chr16:57602433..57603088hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg38656
hg19656
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18185324
Samples
Known GenesGPR114
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507154
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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