A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565208



Internal ID16352617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:76651207..76715959hg38UCSC Ensembl
Innerchr14:77117550..77182302hg19UCSC Ensembl
Innerchr14:76187303..76252055hg18UCSC Ensembl
Cytoband14q24.3
Allele length
AssemblyAllele length
hg3864753
hg1964753
hg1864753
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv829559
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565208
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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