A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1023e199



Internal ID20124325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:62401833..62410076hg38UCSC Ensembl
chr5:61697660..61705903hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg388244
hg198244
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2678311, esv2659593
SamplesNA18602, NA18636
Known GenesDIMT1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1023e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer