A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5867046



Internal ID22641981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64109130..64111704hg38UCSC Ensembl
chr15:64401329..64403903hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg382575
hg192575
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471750
Samples
Known GenesSNX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5867046
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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