A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5834591



Internal ID22609526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:1289770..1294309hg38UCSC Ensembl
chr3:1331454..1335993hg19UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg384540
hg194540
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17489610
Samples
Known GenesCNTN6
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5834591
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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