A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088072



Internal ID21510959
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94172401..94173537hg38UCSC Ensembl
chr14:94638738..94639874hg19UCSC Ensembl
Cytoband14q32.12
Allele length
AssemblyAllele length
hg381137
hg191137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595587
Supporting Variants
SamplesNA24385
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088072
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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