A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv563849



Internal ID16351258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20893225..20952929hg38UCSC Ensembl
Innerchr14:21361384..21421088hg19UCSC Ensembl
Innerchr14:20431224..20490928hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3859705
hg1959705
hg1859705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3540n54
Supporting Variantsnssv823018, nssv823019, nssv823017
Samples
Known GenesECRP
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv563849
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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