A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564198



Internal ID16351607
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34648990..34682878hg38UCSC Ensembl
Innerchr14:35118196..35152084hg19UCSC Ensembl
Innerchr14:34187947..34221835hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3833889
hg1933889
hg1833889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3609n54
Supporting Variantsnssv825161
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564198
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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