A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv946n100



Internal ID22787033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:83998215..84017502hg38UCSC Ensembl
chr10:85757971..85777258hg19UCSC Ensembl
chr10:85747951..85767238hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3819288
hg1919288
hg1819288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1050698, nsv1042775
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv946n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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