A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082213



Internal ID21490443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:96993978..96994632hg38UCSC Ensembl
chr15:97537208..97537862hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg38655
hg19655
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596192
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082213
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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