A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17096671



Internal ID21508526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:75894812..75894874hg38UCSC Ensembl
chr13:76468948..76469010hg19UCSC Ensembl
Cytoband13q22.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5603892
Supporting Variants
SamplesNA20509
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17096671
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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