A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3159n106



Internal ID22796987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117358812..117359137hg38UCSC Ensembl
chr5:116694508..116694833hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38326
hg19326
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1131372, nsv1123030
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv3159n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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