A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17097100



Internal ID21406266
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:57079802..57079981hg38UCSC Ensembl
chr14:57546520..57546699hg19UCSC Ensembl
Cytoband14q22.3
Allele length
AssemblyAllele length
hg38180
hg19180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598386
Supporting Variants
SamplesHG00512
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17097100
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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