A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17394706



Internal ID22452576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:135362148..135362148hg38UCSC Ensembl
chr3:135080990..135080990hg19UCSC Ensembl
Cytoband3q22.2
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5967428
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17394706
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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