A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17085142



Internal ID21446311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:41311822..41312231hg38UCSC Ensembl
chr15:41604020..41604429hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38410
hg19410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5589213
Supporting Variants
SamplesHG00732
Known GenesOIP5
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17085142
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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