A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv242n145



Internal ID22813258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30753371..30757148hg38UCSC Ensembl
chr12:30906305..30910082hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg383778
hg193778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3111572, nsv3117971
Samplessample349, sample348
Known GenesCAPRIN2
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv242n145
Frequency
Sample Size467
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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