A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16292427



Internal ID20501645
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:165920766..165920766hg38UCSC Ensembl
chr2:166777276..166777276hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4753440
Supporting Variants
Samples
Known GenesTTC21B
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16292427
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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