A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv948n100



Internal ID20152564
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:86646619..86714855hg38UCSC Ensembl
chr10:88406376..88474612hg19UCSC Ensembl
chr10:88396356..88464592hg18UCSC Ensembl
Cytoband10q23.2
Allele length
AssemblyAllele length
hg3868237
hg1968237
hg1868237
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036458, nsv1039444
Samples
Known GenesLDB3, OPN4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv948n100
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