A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17380731



Internal ID22438601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74723439..74758382hg38UCSC Ensembl
chr15:75015780..75050723hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3834944
hg1934944
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5935517
Supporting Variants
Samples
Known GenesCYP1A1, CYP1A2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17380731
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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