A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3896n54



Internal ID20137320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:100237676..100241246hg38UCSC Ensembl
chr14:100704013..100707583hg19UCSC Ensembl
chr14:99773766..99777336hg18UCSC Ensembl
Cytoband14q32.2
Allele length
AssemblyAllele length
hg383571
hg193571
hg183571
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv565775, nsv565780
Samples
Known GenesYY1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv3896n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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