A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3520298



Internal ID18471893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46407438..46591179hg38UCSC Ensembl
Innerchr10:46958438..47142310hg19UCSC Ensembl
Innerchr10:46378444..46562316hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38183742
hg19183873
hg18183873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1053859
Supporting Variants
Samples
Known GenesGPRIN2, 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)nssv3520298
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