A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17068119



Internal ID21414720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23111785..23111785hg38UCSC Ensembl
chr10:23400714..23400714hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5625950
Supporting Variants
SamplesHG00513
Known GenesMSRB2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17068119
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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