A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555642



Internal ID15996365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:85977166..86040841hg38UCSC Ensembl
Innerchr11:85688209..85751883hg19UCSC Ensembl
Innerchr11:85365857..85429531hg18UCSC Ensembl
Cytoband11q14.2
Allele length
AssemblyAllele length
hg3863676
hg1963675
hg1863675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2041n54
Supporting Variantsnssv1176189
SamplesHGDP00517
Known GenesPICALM
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555642
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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