A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060052



Internal ID18802583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10338676..10578383hg38UCSC Ensembl
Innerchr21:10934074..11173781hg19UCSC Ensembl
Innerchr21:9955945..10195652hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38239708
hg19239708
hg18239708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3585048
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)nsv1060052
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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