A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555349



Internal ID15996072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:70136918..70137406hg38UCSC Ensembl
Innerchr11:69983024..69983512hg19UCSC Ensembl
Innerchr11:69660672..69661160hg18UCSC Ensembl
Cytoband11q13.3
Allele length
AssemblyAllele length
hg38489
hg19489
hg18489
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1993n54
Supporting Variantsnssv778856, nssv778855, nssv778854
Samples
Known GenesANO1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555349
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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