A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1036n106



Internal ID20160393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108214752..108215552hg38UCSC Ensembl
chr13:108867100..108867900hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38801
hg19801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1143599, nsv1136174
SamplesKWS2, KWS1
Known GenesLIG4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv1036n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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