A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6392233



Internal ID21049786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:100141995..100147531hg38UCSC Ensembl
chr4:101063152..101068688hg19UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg385537
hg195537
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18106809
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6392233
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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