A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17095881



Internal ID21430768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:99790836..99790836hg38UCSC Ensembl
chr15:100331041..100331041hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38130
hg19130
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5662428
Supporting Variants
SamplesHG00731
Known GenesDNM1P46
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17095881
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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