A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17087390



Internal ID21502452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:20828565..20828632hg38UCSC Ensembl
chr14:21296724..21296791hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3868
hg1968
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5593227
Supporting Variants
SamplesNA19239
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17087390
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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