A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv546874



Internal ID15987597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:97995887..98099180hg38UCSC Ensembl
Innerchr1:98461443..98564736hg19UCSC Ensembl
Innerchr1:98234031..98337324hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg38103294
hg19103294
hg18103294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv719637
Samples
Known GenesMIR137, MIR137HG, MIR2682
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv546874
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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