A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564029



Internal ID16351438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:22509594..22535762hg38UCSC Ensembl
Innerchr14:22978577..23004710hg19UCSC Ensembl
Innerchr14:22048417..22074550hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3826169
hg1926134
hg1826134
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv824341
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564029
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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