A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524468



Internal ID15105075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:3212114..3222137hg38UCSC Ensembl
Innerchr11:3233344..3243367hg19UCSC Ensembl
Innerchr11:3189920..3199943hg18UCSC Ensembl
Innerchr11:3189920..3199943hg17UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3810024
hg1910024
hg1810024
hg1710024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700405
Samples
Known GenesMRGPRG, MRGPRG-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524468
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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