A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5893995



Internal ID22669063
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:9086726..9086804hg38UCSC Ensembl
chr3:9128410..9128488hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17411776
Samples
Known GenesSRGAP3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5893995
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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