A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4932n100



Internal ID22791019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:162148105..162247989hg38UCSC Ensembl
chr3:161865893..161965777hg19UCSC Ensembl
chr3:163348587..163448471hg18UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg3899885
hg1999885
hg1899885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1001580, nsv1003997, nsv1011295, nsv1003136, nsv998584, nsv1003824, nsv1004923, nsv1014672, nsv997546, nsv1007722, nsv1014166, nsv1002216, nsv1002803, nsv1012890, nsv1000600, nsv1000759, nsv1000687, nsv1007262, nsv998915
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)dgv4932n100
Frequency
Sample Size11257
Observed Gain45
Observed Loss0
Observed Complex0
Frequencyn/a


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