A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17359620



Internal ID22585289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17709963..17709963hg38UCSC Ensembl
chr10:17751962..17751962hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5951449
Supporting Variants
Samples
Known GenesSTAM
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17359620
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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