A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17090863



Internal ID21463995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:47261424..47261424hg38UCSC Ensembl
chr17:45338790..45338790hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5654932
Supporting Variants
SamplesHG03065
Known GenesITGB3
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17090863
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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