A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431933



Internal ID21089486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133325367..133328670hg38UCSC Ensembl
chr7:133010121..133013424hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg383304
hg193304
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233069
Samples
Known GenesEXOC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431933
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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