A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17412183



Internal ID22470053
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188602177..188602177hg38UCSC Ensembl
chr3:188319965..188319965hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5950519
Supporting Variants
Samples
Known GenesLPP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17412183
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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