A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389641



Internal ID21047194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:125370037..127662951hg38UCSC Ensembl
chr4:126291192..128584106hg19UCSC Ensembl
Cytoband4q28.1
Allele length
AssemblyAllele length
hg382292915
hg192292915
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210265
Samples
Known GenesFAT4, INTU, MIR2054
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389641
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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