A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053859



Internal ID18796390
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 StatusM
Merged Variantsdgv753n100
Supporting Variantsnssv3520298
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)nsv1053859
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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