A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391489



Internal ID21049042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:76112224..76192203hg38UCSC Ensembl
chr4:77033377..77113356hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg3879980
hg1979980
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212383
Samples
Known GenesART3, NUP54, SCARB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391489
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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