A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv951973



Internal ID15899243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:21732084..21832190hg38UCSC Ensembl
Innerchr22:22086373..22186479hg19UCSC Ensembl
Innerchr22:20416373..20516479hg18UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg38100107
hg19100107
hg18100107
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588322
Supporting Variants
Samples
Known GenesMAPK1, YPEL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv951973
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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