A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566267



Internal ID16353676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474867..105487998hg38UCSC Ensembl
Innerchr14:105941204..105954335hg19UCSC Ensembl
Innerchr14:105012249..105025380hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3813132
hg1913132
hg1813132
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3999n54
Supporting Variantsnssv834933
Samples
Known GenesCRIP1, CRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566267
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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