A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1174765



Internal ID15880464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:25150539..25579196hg38UCSC Ensembl
Innerchr11:25172085..25600742hg19UCSC Ensembl
Innerchr11:25128661..25557318hg18UCSC Ensembl
Cytoband11p14.3
Allele length
AssemblyAllele length
hg38428658
hg19428658
hg18428658
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv553860
Supporting Variants
SamplesNINDS_214
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1174765
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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