A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059929



Internal ID18802460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10420986..10558343hg38UCSC Ensembl
Innerchr21:10954114..11091471hg19UCSC Ensembl
Innerchr21:9975985..10113342hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38137358
hg19137358
hg18137358
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4367n100
Supporting Variantsnssv3585073
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5, TPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059929
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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