A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063631



Internal ID18806162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10338676..10510446hg38UCSC Ensembl
Innerchr21:11002011..11173781hg19UCSC Ensembl
Innerchr21:10023882..10195652hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38171771
hg19171771
hg18171771
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4368n100
Supporting Variantsnssv3585154, nssv3585152, nssv3585149, nssv3585151, nssv3585153, nssv3585150, nssv3585155, nssv3585148
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)nsv1063631
Frequency
Sample Size29084
Observed Gain7
Observed Loss1
Observed Complex0
Frequencyn/a


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