A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018960



Internal ID18761493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31478589..31513522hg38UCSC Ensembl
Innerchr6:31446366..31481299hg19UCSC Ensembl
Innerchr6:31554345..31589278hg18UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3834934
hg1934934
hg1834934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655899, nssv3655900, nssv3655898
Samples
Known GenesMICB
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018960
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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