A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564904



Internal ID16352313
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:63879472..63950180hg38UCSC Ensembl
Innerchr14:64346190..64416898hg19UCSC Ensembl
Innerchr14:63415943..63486651hg18UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg3870709
hg1970709
hg1870709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv828237
Samples
Known GenesSYNE2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564904
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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