A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050886



Internal ID18793417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46436509..46631445hg38UCSC Ensembl
Innerchr10:46918172..47113250hg19UCSC Ensembl
Innerchr10:46338178..46533256hg18UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38194937
hg19195079
hg18195079
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv753n100
Supporting Variantsnssv3517419
Samples
Known GenesFAM35BP, GPRIN2, 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)nsv1050886
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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