A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1022n106



Internal ID22794850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99025992..99026097hg38UCSC Ensembl
chr13:99678246..99678351hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg38106
hg19106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1138258, nsv1124729
SamplesKWS2, KWS1
Known GenesDOCK9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1022n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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