A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv759n100



Internal ID20152375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46553641..46606240hg38UCSC Ensembl
chr10:46943377..46995976hg19UCSC Ensembl
chr10:46363383..46415982hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3852600
hg1952600
hg1852600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1042057, nsv1045126
Samples
Known GenesGPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv759n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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