A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv677n100



Internal ID20152293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14305146..14338953hg38UCSC Ensembl
chr10:14347145..14380952hg19UCSC Ensembl
chr10:14387151..14420958hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3833808
hg1933808
hg1833808
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037322, nsv1036071
Samples
Known GenesFRMD4A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv677n100
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