A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv952697



Internal ID16246653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:23683585..23685005hg38UCSC Ensembl
Innerchr22:24025772..24027192hg19UCSC Ensembl
Innerchr22:22355772..22357192hg18UCSC Ensembl
Cytoband22q11.23
Allele length
AssemblyAllele length
hg381421
hg191421
hg181421
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588628
Supporting Variants
Samples
Known GenesGUSBP11
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv952697
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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