A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6393675



Internal ID21051228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:104224616..104242382hg38UCSC Ensembl
chr4:105145773..105163539hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3817767
hg1917767
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209463
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6393675
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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