A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275244



Internal ID20484462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:45890269..45890269hg38UCSC Ensembl
chr3:45931761..45931761hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38235
hg19235
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4754518
Supporting Variants
Samples
Known GenesCCR9, LZTFL1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275244
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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