A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588745



Internal ID16376154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:24836098..24888862hg38UCSC Ensembl
Innerchr22:25232065..25284829hg19UCSC Ensembl
Innerchr22:23562065..23614829hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3852765
hg1952765
hg1852765
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv954321
Samples
Known GenesSGSM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588745
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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