A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3732544



Internal ID18684139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10338676..10558343hg38UCSC Ensembl
Innerchr21:10954114..11173781hg19UCSC Ensembl
Innerchr21:9975985..10195652hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38219668
hg19219668
hg18219668
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065874
Supporting Variants
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)nssv3732544
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer