A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086484



Internal ID21444167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:38477227..38477227hg38UCSC Ensembl
chr15:38769428..38769428hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5648216
Supporting Variants
SamplesHG00732
Known GenesFAM98B
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086484
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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