A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17471785



Internal ID22529677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74722085..74731015hg38UCSC Ensembl
chr15:75014426..75023356hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg388931
hg198931
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5853633
Supporting Variants
Samples
Known GenesCYP1A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17471785
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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