A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069900



Internal ID21452427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17971268..17971268hg38UCSC Ensembl
chr10:18260197..18260197hg19UCSC Ensembl
Cytoband10p12.33
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5634906
Supporting Variants
SamplesHG01596
Known GenesSLC39A12
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069900
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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