A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17417965



Internal ID22475835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:153906965..153906965hg38UCSC Ensembl
chr3:153624754..153624754hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5957794
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17417965
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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