A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080886



Internal ID21454469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80146992..80147047hg38UCSC Ensembl
chr17:78120791..78120846hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5586351
Supporting Variants
SamplesHG02011
Known GenesEIF4A3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080886
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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