A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059585



Internal ID18802116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10386269..10529640hg38UCSC Ensembl
Innerchr21:10982817..11126188hg19UCSC Ensembl
Innerchr21:10004688..10148059hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38143372
hg19143372
hg18143372
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4370n100
Supporting Variantsnssv3585108
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)nsv1059585
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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