A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097791



Internal ID21480694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:101773471..101781934hg38UCSC Ensembl
chr15:102313674..102322137hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg388464
hg198464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5597490
Supporting Variants
SamplesHG03683
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097791
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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