A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16278991



Internal ID20488209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9898367..9899602hg38UCSC Ensembl
chr1:9958425..9959660hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg381236
hg191236
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744322
Supporting Variants
Samples
Known GenesCTNNBIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16278991
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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