A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041036



Internal ID18783567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46481988..46878295hg38UCSC Ensembl
Innerchr10:46674168..47067469hg19UCSC Ensembl
Innerchr10:46094174..46487475hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38396308
hg19393302
hg18393302
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv743n100
Supporting Variantsnssv3506046, nssv3510715
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)nsv1041036
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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