A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066344



Internal ID18808875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10404321..10510446hg38UCSC Ensembl
Innerchr21:11002011..11108136hg19UCSC Ensembl
Innerchr21:10023882..10130007hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38106126
hg19106126
hg18106126
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4370n100
Supporting Variantsnssv3732550
Samples
Known GenesBAGE, BAGE2, BAGE3, BAGE4, BAGE5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066344
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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