A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1773n106



Internal ID19019882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:35116772..35116837hg38UCSC Ensembl
chr19:35607676..35607741hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV tandem duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1142938, nsv1111170
SamplesKWS1, KWS2
Known GenesFXYD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1773n106
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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