A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272686



Internal ID20481904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:123936092..123936092hg38UCSC Ensembl
chr10:125695608..125695608hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4764570
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272686
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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