A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17088849



Internal ID21478448
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:37415232..37415584hg38UCSC Ensembl
chr17:35775316..35775668hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38353
hg19353
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5601094
Supporting Variants
SamplesHG03486
Known GenesTADA2A
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17088849
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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