A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393519



Internal ID21051072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:173329301..173338700hg38UCSC Ensembl
chr4:174250452..174259851hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg389400
hg199400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18214640
Samples
Known GenesHMGB2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393519
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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