A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv571452



Internal ID16012175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10907520..10936885hg38UCSC Ensembl
Innerchr16:11001377..11030742hg19UCSC Ensembl
Innerchr16:10908878..10938243hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg3829366
hg1929366
hg1829366
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv852528
Samples
Known GenesCIITA, DEXI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv571452
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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