A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6407905



Internal ID21065458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87115101..87170100hg38UCSC Ensembl
chr6:87824819..87879818hg19UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3855000
hg1955000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6305n223
Supporting Variantsnssv18221217
Samples
Known GenesZNF292
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6407905
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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