A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6367877



Internal ID21025430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:5106230..5268387hg38UCSC Ensembl
chr4:5107957..5270114hg19UCSC Ensembl
Cytoband4p16.2
Allele length
AssemblyAllele length
hg38162158
hg19162158
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18211884
Samples
Known GenesSTK32B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6367877
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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