A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049850



Internal ID18792381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46428386..46487142hg38UCSC Ensembl
Innerchr10:47062299..47121369hg19UCSC Ensembl
Innerchr10:46482305..46541375hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3858757
hg1959071
hg1859071
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv815n100
Supporting Variantsnssv3705858, nssv3504946, nssv3705856, nssv3705857
Samples
Known GenesLINC00842, LOC100996758, NPY4R
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049850
Frequency
Sample Size29084
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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