A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6379185



Internal ID21036738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:64428101..64500000hg38UCSC Ensembl
chr4:65293819..65365718hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3871900
hg1971900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5298n223
Supporting Variantsnssv18211562
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6379185
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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