A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv566207



Internal ID16006930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:105458373..105474172hg38UCSC Ensembl
Innerchr14:105924710..105940509hg19UCSC Ensembl
Innerchr14:104995755..105011554hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3815800
hg1915800
hg1815800
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv834806
Samples
Known GenesCRIP2, MTA1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv566207
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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