A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566047



Internal ID16006770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104557175..104703666hg38UCSC Ensembl
Innerchr14:105023512..105170003hg19UCSC Ensembl
Innerchr14:104094557..104241048hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg38146492
hg19146492
hg18146492
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148711
SamplesHGDP00696
Known GenesC14orf180, INF2, MIR4710, TMEM179
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566047
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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