A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408998



Internal ID21066551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:96293391..96293873hg38UCSC Ensembl
chr5:95629095..95629577hg19UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38483
hg19483
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215432
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408998
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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