A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376392



Internal ID21033945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:39179581..39183058hg38UCSC Ensembl
chr5:39179683..39183160hg19UCSC Ensembl
Cytoband5p13.1
Allele length
AssemblyAllele length
hg383478
hg193478
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213456
Samples
Known GenesFYB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376392
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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