A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566205



Internal ID16006928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105384700..105454534hg38UCSC Ensembl
Innerchr14:105851037..105920871hg19UCSC Ensembl
Innerchr14:104922082..104991916hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3869835
hg1969835
hg1869835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834805
Samples
Known GenesMTA1, PACS2, TEX22
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566205
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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