A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834398



Internal ID15781668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:103541218..103626452hg38UCSC Ensembl
Innerchr14:104007555..104092789hg19UCSC Ensembl
Innerchr14:103077308..103162542hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3885235
hg1985235
hg1885235
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566022
Supporting Variants
Samples
Known GenesAPOPT1, BAG5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834398
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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