A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391076



Internal ID21048629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:152484392..152510089hg38UCSC Ensembl
chr4:153405544..153431241hg19UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg3825698
hg1925698
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18112024
Samples
Known GenesFBXW7, MIR3140
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391076
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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