A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564414



Internal ID16351823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:38489763..38589718hg38UCSC Ensembl
Innerchr14:38958967..39058922hg19UCSC Ensembl
Innerchr14:38028718..38128673hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3899956
hg1999956
hg1899956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3649n54
Supporting Variantsnssv826030
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564414
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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