A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6394239



Internal ID21051792
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:166329893..166338263hg38UCSC Ensembl
chr4:167251045..167259415hg19UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg388371
hg198371
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213810
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6394239
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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