A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409506



Internal ID21067059
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35345559..35359655hg38UCSC Ensembl
chr6:35313336..35327432hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg3814097
hg1914097
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219245
Samples
Known GenesPPARD
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409506
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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