A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526229



Internal ID15453522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:18918119..18953313hg38UCSC Ensembl
Innerchr11:18939666..18974860hg19UCSC Ensembl
Innerchr11:18896242..18931436hg18UCSC Ensembl
Innerchr11:18896242..18931436hg17UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg3835195
hg1935195
hg1835195
hg1735195
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702495
Samples
Known GenesMRGPRX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526229
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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