A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17411171



Internal ID22469041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:42856915..42856915hg38UCSC Ensembl
chr3:42898407..42898407hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961680
Supporting Variants
Samples
Known GenesACKR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17411171
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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