A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16283188



Internal ID20492406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112913189..112913282hg38UCSC Ensembl
chr10:114672948..114673041hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4749648
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16283188
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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