A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17552675



Internal ID21877030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193992925..193992925hg38UCSC Ensembl
chr3:193710714..193710714hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6074655
Supporting Variants
Samples
Known GenesLOC647323
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17552675
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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