A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359137



Internal ID21016690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:165293801..165366300hg38UCSC Ensembl
chr3:165011589..165084088hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3872500
hg1972500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208522
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359137
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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