A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17092269



Internal ID21491978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:39315744..39315803hg38UCSC Ensembl
chr13:39889881..39889940hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602497
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17092269
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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