A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv591268



Internal ID16378677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:109476199..109662581hg38UCSC Ensembl
Innerchr3:109195046..109381428hg19UCSC Ensembl
Innerchr3:110677736..110864118hg18UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg38186383
hg19186383
hg18186383
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1152521
SamplesHGDP01179
Known GenesFLJ25363
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv591268
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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