A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17089080



Internal ID21454771
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:94989653..94991762hg38UCSC Ensembl
chr14:95455990..95458099hg19UCSC Ensembl
Cytoband14q32.13
Allele length
AssemblyAllele length
hg382110
hg192110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588504
Supporting Variants
SamplesHG02011
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17089080
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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