A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17543397



Internal ID21867752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:177457361..177457361hg38UCSC Ensembl
chr3:177175149..177175149hg19UCSC Ensembl
Cytoband3q26.32
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061681
Supporting Variants
Samples
Known GenesLINC00578
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17543397
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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