A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv695n100



Internal ID22786782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:26936975..26957892hg38UCSC Ensembl
chr10:27225904..27246821hg19UCSC Ensembl
chr10:27265910..27286827hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3820918
hg1920918
hg1820918
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036722, nsv1047111, nsv1043456
Samples
Known GenesLINC00202-1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv695n100
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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