A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546901



Internal ID16334310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:102143021..102251454hg38UCSC Ensembl
Innerchr1:102608577..102717010hg19UCSC Ensembl
Innerchr1:102381165..102489598hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38108434
hg19108434
hg18108434
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv719680
Samples
Known GenesMIR548AI
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546901
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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