A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv589053



Internal ID16029776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:41909579..41928618hg38UCSC Ensembl
Innerchr22:42305583..42324622hg19UCSC Ensembl
Innerchr22:40635529..40654568hg18UCSC Ensembl
Cytoband22q13.2
Allele length
AssemblyAllele length
hg3819040
hg1919040
hg1819040
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv957091
Samples
Known GenesSHISA8, TNFRSF13C
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv589053
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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