A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv651n145



Internal ID22813667
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:143835616..143839122hg38UCSC Ensembl
chr2:144593185..144596691hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg383507
hg193507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3113371, nsv3114175, nsv3118143, nsv3110827, nsv3113684, nsv3112588, nsv3110977, nsv3117998, nsv3114327, nsv3112265
Samplessample37, sample230, sample98, sample159, sample380, sample50, sample329, sample369, sample206, sample353, sample332, sample293, sample395, sample102, sample112, sample117, sample234, sample155
Known Genes
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv651n145
Frequency
Sample Size467
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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