A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16262384



Internal ID20471602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129779873..129779873hg38UCSC Ensembl
chr10:131578137..131578137hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38234
hg19234
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4750308
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16262384
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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