A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045466



Internal ID18787997
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46432210..47008602hg38UCSC Ensembl
Innerchr10:46543845..47117543hg19UCSC Ensembl
Innerchr10:45963851..46537549hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38576393
hg19573699
hg18573699
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv734n100
Supporting Variantsnssv3508271
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, LINC00842, LOC100996758, NPY4R, PTPN20A, PTPN20B, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1045466
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