A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090214



Internal ID21459260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:102877040..102877541hg38UCSC Ensembl
chr14:103343377..103343878hg19UCSC Ensembl
Cytoband14q32.32
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5596894
Supporting Variants
SamplesHG02818
Known GenesTRAF3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090214
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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