A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065874



Internal ID19155093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10338676..10558343hg38UCSC Ensembl
Innerchr21:10954114..11173781hg19UCSC Ensembl
Innerchr21:9975985..10195652hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38219668
hg19219668
hg18219668
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4368n100
Supporting Variantsnssv3732544, nssv3585081, nssv3585082, nssv3585078, nssv3585075, nssv3585079, nssv3585080, nssv3585083, nssv3585076, nssv3585077
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)nsv1065874
Frequency
Sample Size11257
Observed Gain9
Observed Loss1
Observed Complex0
Frequencyn/a


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