A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483084



Internal ID15235558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr11:78645595..78818126hg38UCSC Ensembl
Innerchr11:78356640..78529171hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38172532
hg19172532
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996328
Samples
Known GenesTENM4
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483084
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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