A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1719n106



Internal ID20161076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:14852273..14903469hg38UCSC Ensembl
chr19:14963085..15014281hg19UCSC Ensembl
Cytoband19p13.12
Allele length
AssemblyAllele length
hg3851197
hg1951197
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1112313, nsv1142037
SamplesKWS2, KWS1
Known GenesOR7A17
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1719n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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