A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092609



Internal ID21501346
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:74421627..74425871hg38UCSC Ensembl
chr15:74713968..74718212hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg384245
hg194245
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5667909
Supporting Variants
SamplesNA19239
Known GenesSEMA7A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092609
Frequency
Sample Size35
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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