A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6390860



Internal ID21048413
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:62498850..62524707hg38UCSC Ensembl
chr4:63364568..63390425hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3825858
hg1925858
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18118550
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6390860
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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