A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv553967



Internal ID16341376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:31372799..31375414hg38UCSC Ensembl
Innerchr11:31394346..31396961hg19UCSC Ensembl
Innerchr11:31350922..31353537hg18UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg382616
hg192616
hg182616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1737n54
Supporting Variantsnssv770968, nssv770969
Samples
Known GenesDNAJC24
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv553967
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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