A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5660650



Internal ID21608955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:100058245..100058245hg38UCSC Ensembl
chr15:100598450..100598450hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38491
hg19491
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17090969, nssv17099092
SamplesNA19238, HG00731
Known GenesADAMTS17
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5660650
Frequency
Sample Size35
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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