A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4771n100



Internal ID22790858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:68666567..68698250hg38UCSC Ensembl
chr3:68715718..68747401hg19UCSC Ensembl
chr3:68798408..68830091hg18UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3831684
hg1931684
hg1831684
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1008984, nsv1006954, nsv1005544, nsv998856
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv4771n100
Frequency
Sample Size11257
Observed Gain29
Observed Loss136
Observed Complex0
Frequencyn/a


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