A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv747n100



Internal ID20152363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46554143..46631445hg38UCSC Ensembl
chr10:46918172..46995474hg19UCSC Ensembl
chr10:46338178..46415480hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3877303
hg1977303
hg1877303
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1036598, nsv1038276, nsv1041475
Samples
Known GenesFAM35BP, GPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv747n100
Frequency
Sample Size29084
Observed Gain13
Observed Loss18
Observed Complex0
Frequencyn/a


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