A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411639



Internal ID21069192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122509301..122518100hg38UCSC Ensembl
chr5:121844996..121853795hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5928n223
Supporting Variantsnssv18213141
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411639
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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