A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060860



Internal ID19150079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10356385..10775598hg38UCSC Ensembl
Innerchr21:10736859..11156072hg19UCSC Ensembl
Innerchr21:9758730..10177943hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38419214
hg19419214
hg18419214
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4354n100
Supporting Variantsnssv3583783, nssv3583784, nssv3732515
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)nsv1060860
Frequency
Sample Size11257
Observed Gain1
Observed Loss2
Observed Complex0
Frequencyn/a


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