A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046287



Internal ID18788818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46395843..46631445hg38UCSC Ensembl
Innerchr10:46918172..47153919hg19UCSC Ensembl
Innerchr10:46338178..46573925hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38235603
hg19235748
hg18235748
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv753n100
Supporting Variantsnssv3515128, nssv3707891
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)nsv1046287
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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