A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1121n106



Internal ID20160478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:89567499..89567610hg38UCSC Ensembl
chr14:90033843..90033954hg19UCSC Ensembl
Cytoband14q32.11
Allele length
AssemblyAllele length
hg38112
hg19112
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1117931, nsv1135372
SamplesKWS1
Known GenesFOXN3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1121n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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