A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17407769



Internal ID22465639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:104925173..104929997hg38UCSC Ensembl
chr3:104644017..104648841hg19UCSC Ensembl
Cytoband3q13.11
Allele length
AssemblyAllele length
hg384825
hg194825
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5900828
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17407769
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.001


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