A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364851



Internal ID21022404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:1104733..2006628hg38UCSC Ensembl
chr3:1146417..2048312hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg38901896
hg19901896
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4750n223
Supporting Variantsnssv18207243
Samples
Known GenesCNTN6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364851
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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