A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2658n106



Internal ID22796486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:190237605..190237921hg38UCSC Ensembl
chr3:189955394..189955710hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38317
hg19317
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121273, nsv1120818, nsv1144544
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2658n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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