A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566073



Internal ID16353482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104801891..104808426hg38UCSC Ensembl
Innerchr14:105268228..105274763hg19UCSC Ensembl
Innerchr14:104339273..104345808hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg386536
hg196536
hg186536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834454, nssv834455
Samples
Known GenesZBTB42
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566073
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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