A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv929n100



Internal ID20152545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:77596297..77855405hg38UCSC Ensembl
chr10:79356055..79615163hg19UCSC Ensembl
chr10:79026061..79285169hg18UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38259109
hg19259109
hg18259109
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046996, nsv1040785, nsv1041017
Samples
Known GenesDLG5, KCNMA1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv929n100
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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