A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043728



Internal ID18786259
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46407438..46631445hg38UCSC Ensembl
Innerchr10:46918172..47142310hg19UCSC Ensembl
Innerchr10:46338178..46562316hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38224008
hg19224139
hg18224139
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv753n100
Supporting Variantsnssv3507283
Samples
Known GenesFAM35BP, GPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1043728
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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