A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17093155



Internal ID21492112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:74994740..74995059hg38UCSC Ensembl
chr14:75461443..75461762hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598961
Supporting Variants
SamplesNA19238
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17093155
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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