A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5864012



Internal ID22638947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74740067..74753686hg38UCSC Ensembl
chr15:75032408..75046027hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3813620
hg1913620
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17473624
Samples
Known GenesCYP1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5864012
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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