A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17069928



Internal ID21440533
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18741447..18741596hg38UCSC Ensembl
chr10:19030376..19030525hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5588720
Supporting Variants
SamplesHG00732
Known Genes
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17069928
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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