A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17080282



Internal ID21438919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:43842301..43842376hg38UCSC Ensembl
chr17:41919669..41919744hg19UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5600791
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17080282
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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