A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565026



Internal ID16352435
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:70221529..70222569hg38UCSC Ensembl
Innerchr14:70688246..70689286hg19UCSC Ensembl
Innerchr14:69757999..69759039hg18UCSC Ensembl
Cytoband14q24.2
Allele length
AssemblyAllele length
hg381041
hg191041
hg181041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3748n54
Supporting Variantsnssv828984, nssv828983, nssv828982, nssv828980, nssv828985, nssv828981
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565026
Frequency
Sample Size17421
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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