A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389279



Internal ID21046832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:41716352..41716933hg38UCSC Ensembl
chr4:41718369..41718950hg19UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg38582
hg19582
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18213638
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389279
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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