A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv9025n54



Internal ID22776920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:42704111..42707404hg38UCSC Ensembl
chr4:42706128..42709421hg19UCSC Ensembl
chr4:42400885..42404178hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg383294
hg193294
hg183294
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv594071, nsv594064, nsv594065, nsv594066, nsv594063, nsv594068, nsv594067, nsv594070
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv9025n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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