A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv957226



Internal ID16251182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:47333549..47387702hg38UCSC Ensembl
Innerchr22:47729299..47783452hg19UCSC Ensembl
Innerchr22:46107963..46162116hg18UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3854154
hg1954154
hg1854154
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv589144
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv957226
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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