A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv954523



Internal ID16248479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:25331345..25365969hg38UCSC Ensembl
Innerchr22:25727312..25761936hg19UCSC Ensembl
Innerchr22:24057312..24091936hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg3834625
hg1934625
hg1834625
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588841
Supporting Variants
Samples
Known GenesLRP5L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv954523
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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