A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564349



Internal ID16351758
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:37421228..37565229hg38UCSC Ensembl
Innerchr14:37890433..38034434hg19UCSC Ensembl
Innerchr14:36960184..37104185hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38144002
hg19144002
hg18144002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv825771
Samples
Known GenesMIPOL1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564349
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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