A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546900



Internal ID16334309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:101910702..102008003hg38UCSC Ensembl
Innerchr1:102376258..102473559hg19UCSC Ensembl
Innerchr1:102148846..102246147hg18UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3897302
hg1997302
hg1897302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv719679
Samples
Known GenesMIR548AI, OLFM3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546900
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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