A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16269795



Internal ID20479013
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11196993..11196993hg38UCSC Ensembl
chr10:11238956..11238956hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38189
hg19189
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4763873
Supporting Variants
Samples
Known GenesCELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16269795
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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