A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063227



Internal ID19152446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10510446..10558343hg38UCSC Ensembl
Innerchr21:10954114..11002011hg19UCSC Ensembl
Innerchr21:9975985..10023882hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3847898
hg1947898
hg1847898
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4365n100
Supporting Variantsnssv3732538
Samples
Known GenesTPTE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1063227
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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