A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17540276



Internal ID21864631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196027979..196027979hg38UCSC Ensembl
chr3:195754850..195754850hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6076760
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17540276
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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