A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1731n100



Internal ID19012099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95279115..95386474hg38UCSC Ensembl
chr13:95931369..96038728hg19UCSC Ensembl
chr13:94729370..94836729hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38107360
hg19107360
hg18107360
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047208, nsv1047902, nsv1053262, nsv1040348, nsv1039391, nsv1044162, nsv1036031, nsv1044131, nsv1049988, nsv1042622
Samples
Known GenesABCC4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv1731n100
Frequency
Sample Size29084
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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