A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1045328



Internal ID18787859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:46467768..46878295hg38UCSC Ensembl
Innerchr10:46674168..47081683hg19UCSC Ensembl
Innerchr10:46094174..46501689hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38410528
hg19407516
hg18407516
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv743n100
Supporting Variantsnssv3510069, nssv3507811
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)nsv1045328
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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