A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17596936



Internal ID21788979
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:23111840..23111840hg38UCSC Ensembl
chr10:23400769..23400769hg19UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6091817
Supporting Variants
Samples
Known GenesMSRB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17596936
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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