A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090969



Internal ID21491811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100058245..100058245hg38UCSC Ensembl
chr15:100598450..100598450hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38207
hg19207
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5660650
Supporting Variants
SamplesNA19238
Known GenesADAMTS17
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090969
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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