A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv440n106



Internal ID19018549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46395862..46635417hg38UCSC Ensembl
chr10:46914200..47153900hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38239556
hg19239701
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1141177, nsv1132337
SamplesKWS1, KWS2
Known GenesFAM35BP, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)dgv440n106
Frequency
Sample Size2
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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