A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398281



Internal ID21055834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:95644401..95648900hg38UCSC Ensembl
chr5:94980105..94984604hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg384500
hg194500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215032
Samples
Known GenesRFESD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398281
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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