A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv641n145



Internal ID22813657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:109306595..109316845hg38UCSC Ensembl
chr2:109923051..109933301hg19UCSC Ensembl
Cytoband2q12.3
Allele length
AssemblyAllele length
hg3810251
hg1910251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv3112074, nsv3111456
Samplessample396, sample125, sample42, sample375, sample424, sample130, sample163, sample207
Known GenesMIR4266, SH3RF3
MethodOligo aCGH
Analysis
Platform
Comments
ReferenceLu_et_al_2017
Pubmed ID28705883
Accession Number(s)dgv641n145
Frequency
Sample Size467
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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