A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398391



Internal ID21055944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:458438..782915hg38UCSC Ensembl
chr6:458438..782915hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg38324478
hg19324478
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6041n223
Supporting Variantsnssv18231803
Samples
Known GenesEXOC2, HUS1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398391
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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