A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv555984



Internal ID16343393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:96475095..96534359hg38UCSC Ensembl
Innerchr11:96208259..96267523hg19UCSC Ensembl
Innerchr11:95847907..95907171hg18UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3859265
hg1959265
hg1859265
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2106n54
Supporting Variantsnssv781659, nssv781658
Samples
Known GenesJRKL-AS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv555984
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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