A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564060



Internal ID16004783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:24307195..24340589hg38UCSC Ensembl
Innerchr14:24776401..24809795hg19UCSC Ensembl
Innerchr14:23846241..23879635hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3833395
hg1933395
hg1833395
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv824390
Samples
Known GenesADCY4, CIDEB, LTB4R, LTB4R2, NOP9, RIPK3
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564060
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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