A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17416881



Internal ID22474751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32823690..32823690hg38UCSC Ensembl
chr3:32865182..32865182hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5961966
Supporting Variants
Samples
Known GenesTRIM71
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17416881
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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