A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565880



Internal ID16006603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101539186..101625954hg38UCSC Ensembl
Innerchr14:102005523..102092291hg19UCSC Ensembl
Innerchr14:101075276..101162044hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg3886769
hg1986769
hg1886769
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv833715
Samples
Known GenesDIO3, DIO3OS, MIR1247
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565880
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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