A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17084850



Internal ID21482616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:40386235..40386235hg38UCSC Ensembl
chr15:40678436..40678436hg19UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg38335
hg19335
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5647460
Supporting Variants
SamplesHG03732
Known GenesKNSTRN
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17084850
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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