A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093951



Internal ID21492192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:39894052..39894052hg38UCSC Ensembl
chr15:40186253..40186253hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38322
hg19322
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648109
Supporting Variants
SamplesNA19238
Known GenesGPR176
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093951
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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