A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058078



Internal ID18800609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10427788..10775598hg38UCSC Ensembl
Innerchr21:10736859..11084669hg19UCSC Ensembl
Innerchr21:9758730..10106540hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38347811
hg19347811
hg18347811
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4355n100
Supporting Variantsnssv3583759
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)nsv1058078
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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