A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039540



Internal ID18782071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46538831..46878295hg38UCSC Ensembl
Innerchr10:46674168..47010786hg19UCSC Ensembl
Innerchr10:46094174..46430792hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38339465
hg19336619
hg18336619
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv739n100
Supporting Variantsnssv3506029
Samples
Known GenesBMS1P1, BMS1P5, FAM35BP, FRMPD2P1, GLUD1P7, GPRIN2, SYT15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039540
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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