A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv728n100



Internal ID20152344
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:43225695..43378216hg38UCSC Ensembl
chr10:43721143..43873664hg19UCSC Ensembl
chr10:43041149..43193670hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38152522
hg19152522
hg18152522
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1035873, nsv1044422
Samples
Known GenesFXYD4, RASGEF1A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv728n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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