A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17082504



Internal ID21412936
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:75407798..75408637hg38UCSC Ensembl
chr14:75874501..75875340hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38840
hg19840
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5602083
Supporting Variants
SamplesHG00513
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17082504
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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