A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057818



Internal ID18800349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10338676..10607210hg38UCSC Ensembl
Innerchr21:10905247..11173781hg19UCSC Ensembl
Innerchr21:9927118..10195652hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38268535
hg19268535
hg18268535
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4358n100
Supporting Variantsnssv3585026
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)nsv1057818
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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