A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387861



Internal ID21045414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:104643643..104657276hg38UCSC Ensembl
chr4:105564800..105578433hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3813634
hg1913634
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209469
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387861
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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