A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361503



Internal ID21019056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1693932..1725194hg38UCSC Ensembl
chr4:1695659..1726921hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg3831263
hg1931263
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213867
Samples
Known GenesSLBP, TACC3, TMEM129
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361503
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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