A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4751n100



Internal ID22790838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:60322224..60431606hg38UCSC Ensembl
chr3:60307954..60417339hg19UCSC Ensembl
chr3:60282994..60392379hg18UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38109383
hg19109386
hg18109386
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1011408, nsv1013291, nsv1011133
Samples
Known GenesFHIT
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4751n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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