A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564951



Internal ID16352360
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:65488799..65586183hg38UCSC Ensembl
Innerchr14:65955517..66052901hg19UCSC Ensembl
Innerchr14:65025270..65122654hg18UCSC Ensembl
Cytoband14q23.3
Allele length
AssemblyAllele length
hg3897385
hg1997385
hg1897385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149497
Samples1780862206_A
Known GenesFUT8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564951
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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