A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395066



Internal ID21052619
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:120194414..120210767hg38UCSC Ensembl
chr4:121115569..121131922hg19UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3816354
hg1916354
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210204
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395066
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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