A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv784611



Internal ID15731881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:118608595..118611488hg38UCSC Ensembl
Innerchr11:118479310..118482203hg19UCSC Ensembl
Innerchr11:117984520..117987413hg18UCSC Ensembl
Cytoband11q23.3
Allele length
AssemblyAllele length
hg382894
hg192894
hg182894
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv556465
Supporting Variants
Samples
Known GenesPHLDB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv784611
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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