A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv144n6



Internal ID6314056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:55577816..55577892hg19UCSC Ensembl
chr4:55272573..55272649hg18UCSC Ensembl
chr4:55418744..55418820hg17UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg19n/a
hg18n/a
hg17n/a
Variant TypeCNV Loss
Copy Number
Allele State
Allele Origin
Probe Count
Merged StatusM
Merged Variants
Supporting Variantsnsv290717, nsv289421
Samples
Known GenesKIT
Method
Analysis
Platform
Comments
ReferenceMills et al 2006
Pubmed ID16902084
Accession Number(s)dgv144n6
Frequency
Sample Size24
Observed Gainn/a
Observed Lossn/a
Observed Complexn/a
Frequencyn/a


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