A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2668n106



Internal ID22796496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:193157511..193167616hg38UCSC Ensembl
chr3:192875300..192885405hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3810106
hg1910106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121024, nsv1135606
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2668n106
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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