A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv564811



Internal ID16352220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48106920..48132794hg38UCSC Ensembl
Innerchr14:48576123..48601997hg19UCSC Ensembl
Innerchr14:47645873..47671747hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3825875
hg1925875
hg1825875
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3711n54
Supporting Variantsnssv827840
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv564811
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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