A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527985



Internal ID15455278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:184464020..184533615hg38UCSC Ensembl
Innerchr3:184181808..184251403hg19UCSC Ensembl
Innerchr3:185664502..185734097hg18UCSC Ensembl
Innerchr3:185664510..185734105hg17UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg3869596
hg1969596
hg1869596
hg1769596
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704504
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527985
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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