A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406286



Internal ID21063839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117827893..117844452hg38UCSC Ensembl
chr5:117163588..117180147hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3816560
hg1916560
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212490
Samples
Known GenesLOC102467224
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406286
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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