A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412358



Internal ID21069911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:128667787..128669877hg38UCSC Ensembl
chr5:128003480..128005570hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg382091
hg192091
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215413
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412358
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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