A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv915007



Internal ID6276934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:36675150..36722490hg19UCSC Ensembl
Outerchr22:36672276..36725970hg19UCSC Ensembl
Innerchr22:35005096..35052436hg18UCSC Ensembl
Outerchr22:35002222..35055916hg18UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusS
Merged Variants
Supporting Variantsnssv1547103
SamplesMS17208
Known GenesMYH9
Method
Analysis
PlatformIllumina HumanHap 610 Quad + Illumina HumanHap 1MduoV3
Comments
ReferenceXu_et_al_2011
Pubmed ID21882294
Accession Number(s)nsv915007
Frequency
Sample Size6533
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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