A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6423289



Internal ID21080842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133274602..133309236hg38UCSC Ensembl
chr7:132959357..132993990hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3834635
hg1934634
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18224354
Samples
Known GenesEXOC4, MIR6133
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6423289
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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