A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068399



Internal ID21414582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119519593..119519672hg38UCSC Ensembl
chr10:121279105..121279184hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3880
hg1980
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5598100
Supporting Variants
SamplesHG00513
Known GenesRGS10
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068399
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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