A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv764302



Internal ID16058258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:1560577..1568925hg38UCSC Ensembl
Innerchr11:1581807..1590155hg19UCSC Ensembl
Innerchr11:1538383..1546731hg18UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg388349
hg198349
hg188349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552997
Supporting Variants
Samples
Known GenesDUSP8, MOB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv764302
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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