A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv868n100



Internal ID22786955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:55943048..56009533hg38UCSC Ensembl
chr10:57702808..57769294hg19UCSC Ensembl
chr10:57372814..57439300hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3866486
hg1966487
hg1866487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1038656, nsv1042268
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)dgv868n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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