A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564480



Internal ID16351889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:41136353..41209263hg38UCSC Ensembl
Innerchr14:41605556..41678466hg19UCSC Ensembl
Innerchr14:40675306..40748216hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3872911
hg1972911
hg1872911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3659n54
Supporting Variantsnssv826691, nssv826692, nssv826693
Samples
Known GenesLOC644919
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564480
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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