A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5853633



Internal ID22628568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74722085..74731015hg38UCSC Ensembl
chr15:75014426..75023356hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg388931
hg198931
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17471785
Samples
Known GenesCYP1A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5853633
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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