A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389942



Internal ID21047495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:99949401..99951600hg38UCSC Ensembl
chr4:100870558..100872757hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg382200
hg192200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214425
Samples
Known GenesH2AFZ, LOC256880
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389942
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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