A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4784n100



Internal ID22790871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:75400451..75600071hg38UCSC Ensembl
chr3:75449602..75649222hg19UCSC Ensembl
chr3:75532292..75731912hg18UCSC Ensembl
Cytoband3p12.3
Allele length
AssemblyAllele length
hg38199621
hg19199621
hg18199621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1006072, nsv1003370, nsv1013458, nsv1011531, nsv1008128, nsv1010289, nsv1009002, nsv1011950, nsv998282, nsv998176, nsv1008151, nsv1004798, nsv1007079
Samples
Known GenesFAM86DP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4784n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss30
Observed Complex0
Frequencyn/a


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