A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17086339



Internal ID21434495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:76347430..76347864hg38UCSC Ensembl
chr14:76813773..76814207hg19UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg38435
hg19435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5595549
Supporting Variants
SamplesHG00731
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17086339
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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