A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17148284



Internal ID21481439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17695982..17698710hg38UCSC Ensembl
chr6:17696213..17698941hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg382729
hg192729
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5573312
Supporting Variants
SamplesHG03683
Known GenesNUP153
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17148284
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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