A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5836576



Internal ID22611511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:47261602..47263701hg38UCSC Ensembl
chr3:47303092..47305191hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg382100
hg192100
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17491571, nssv17491570
Samples
Known GenesKIF9
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5836576
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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