A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1770n106



Internal ID22795598
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:33249758..33250625hg38UCSC Ensembl
chr19:33740664..33741531hg19UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg38868
hg19868
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1125671, nsv1111168
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1770n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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