A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1682n106



Internal ID19019791
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1137101..1138301hg38UCSC Ensembl
chr19:1137100..1138300hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1112733, nsv1144849
SamplesKWS1, KWS2
Known GenesSBNO2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1682n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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