A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv588886



Internal ID16029609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:30440326..30472431hg38UCSC Ensembl
Innerchr22:30836313..30868418hg19UCSC Ensembl
Innerchr22:29166313..29198418hg18UCSC Ensembl
Cytoband22q12.2
Allele length
AssemblyAllele length
hg3832106
hg1932106
hg1832106
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv954560
Samples
Known GenesSEC14L3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv588886
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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