A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv807n100



Internal ID20152423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46332711..46489856hg38UCSC Ensembl
chr10:47055642..47249575hg19UCSC Ensembl
chr10:46475648..46669581hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38157146
hg19193934
hg18193934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1054830, nsv1038522, nsv1052088, nsv1040690
Samples
Known GenesAGAP9, ANXA8, BMS1P2, BMS1P6, FAM25C, FAM25G, HNRNPA1P33, LINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv807n100
Frequency
Sample Size29084
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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