A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566266



Internal ID16353675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105474867..105480505hg38UCSC Ensembl
Innerchr14:105941204..105946842hg19UCSC Ensembl
Innerchr14:105012249..105017887hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg385639
hg195639
hg185639
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3991n54
Supporting Variantsnssv834932
Samples
Known GenesCRIP2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566266
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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