A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523703



Internal ID15450996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3220993..3232626hg38UCSC Ensembl
Innerchr11:3242223..3253856hg19UCSC Ensembl
Innerchr11:3198799..3210432hg18UCSC Ensembl
Innerchr11:3198799..3210432hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3811634
hg1911634
hg1811634
hg1711634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699511
Samples
Known GenesMRGPRE, MRGPRG-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523703
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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