A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17083645



Internal ID21435753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:65802179..65802179hg38UCSC Ensembl
chr15:66094517..66094517hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5651201
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17083645
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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