A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv834449



Internal ID15781719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:104706874..104719230hg38UCSC Ensembl
Innerchr14:105173211..105185567hg19UCSC Ensembl
Innerchr14:104244256..104256612hg18UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg3812357
hg1912357
hg1812357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv566068
Supporting Variants
Samples
Known GenesINF2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv834449
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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