A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526490



Internal ID15453783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:155748143..155749280hg38UCSC Ensembl
Innerchr3:155465932..155467069hg19UCSC Ensembl
Innerchr3:156948626..156949763hg18UCSC Ensembl
Innerchr3:156948634..156949771hg17UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg381138
hg191138
hg181138
hg171138
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv303n21
Supporting Variantsnssv702799
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526490
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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