A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4707n100



Internal ID20156323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:25597903..25651960hg38UCSC Ensembl
chr3:25639394..25693451hg19UCSC Ensembl
chr3:25614398..25668455hg18UCSC Ensembl
Cytoband3p24.2
Allele length
AssemblyAllele length
hg3854058
hg1954058
hg1854058
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1009374, nsv1000991
Samples
Known GenesRARB, TOP2B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4707n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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