A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16282404



Internal ID20491622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:167148392..167148392hg38UCSC Ensembl
chr2:168004902..168004902hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767887
Supporting Variants
Samples
Known GenesXIRP2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16282404
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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