A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv660n100



Internal ID20152276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:2641472..3092489hg38UCSC Ensembl
chr10:2683664..3134681hg19UCSC Ensembl
chr10:2673664..3124681hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg38451018
hg19451018
hg18451018
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1040966, nsv1052921, nsv1043635, nsv1044287, nsv1043848, nsv1054918, nsv1035593, nsv1049655, nsv1042698, nsv1044605, nsv1041950, nsv1053719, nsv1046501, nsv1037173
Samples
Known GenesPFKP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv660n100
Frequency
Sample Size29084
Observed Gain25
Observed Loss0
Observed Complex0
Frequencyn/a


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