A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17556123



Internal ID21880478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:78082102..78082102hg38UCSC Ensembl
chr3:78131253..78131253hg19UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38291
hg19291
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061477
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17556123
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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