A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565490



Internal ID16352899
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:86048831..86159910hg38UCSC Ensembl
Innerchr14:86515175..86626254hg19UCSC Ensembl
Innerchr14:85584928..85696007hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg38111080
hg19111080
hg18111080
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149532
SamplesHGDP00613
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565490
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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