A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411435



Internal ID21068988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132122232..132159337hg38UCSC Ensembl
chr5:131457925..131495030hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3837106
hg1937106
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18215853
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411435
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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