A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8904n54



Internal ID20142328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:1870601..1872507hg38UCSC Ensembl
chr4:1872328..1874234hg19UCSC Ensembl
chr4:1842126..1844032hg18UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg381907
hg191907
hg181907
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv593354, nsv593343
Samples
Known GenesWHSC1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv8904n54
Frequency
Sample Size17421
Observed Gain3
Observed Loss4
Observed Complex0
Frequencyn/a


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