A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564195



Internal ID16351604
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:34638751..34684785hg38UCSC Ensembl
Innerchr14:35107957..35153991hg19UCSC Ensembl
Innerchr14:34177708..34223742hg18UCSC Ensembl
Cytoband14q13.1
Allele length
AssemblyAllele length
hg3846035
hg1946035
hg1846035
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3609n54
Supporting Variantsnssv825156
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564195
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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