A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092127



Internal ID21475960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96924082..96924947hg38UCSC Ensembl
chr15:97467312..97468177hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38866
hg19866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588260
Supporting Variants
SamplesHG03486
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092127
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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