A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424533



Internal ID21082086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133483212..133509080hg38UCSC Ensembl
chr7:133167966..133193834hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3825869
hg1925869
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18228302
Samples
Known GenesEXOC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424533
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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