A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546898



Internal ID15987621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:101808720..101838596hg38UCSC Ensembl
Innerchr1:102274276..102304152hg19UCSC Ensembl
Innerchr1:102046864..102076740hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3829877
hg1929877
hg1829877
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv379n54
Supporting Variantsnssv719677
Samples
Known GenesOLFM3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546898
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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