A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv954604



Internal ID16248560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:31024156..31032867hg38UCSC Ensembl
Innerchr22:31420142..31428853hg19UCSC Ensembl
Innerchr22:29750142..29758853hg18UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg388712
hg198712
hg188712
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv588891
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)nssv954604
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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