A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv2618n106



Internal ID22796446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148849005..148849335hg38UCSC Ensembl
chr3:148566792..148567122hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38331
hg19331
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1121268, nsv1111621, nsv1119347, nsv1119832
SamplesKWS2, KWS1
Known GenesCPB1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv2618n106
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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