A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276262



Internal ID20485480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:151769244..151769244hg38UCSC Ensembl
chr1:151741720..151741720hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4758017
Supporting Variants
Samples
Known GenesOAZ3
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276262
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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