A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6413642



Internal ID21071195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:75600801..75603000hg38UCSC Ensembl
chr6:76310517..76312716hg19UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18235145
Samples
Known GenesSENP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6413642
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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