A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585058



Internal ID18883339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10509823..10558343hg38UCSC Ensembl
Innerchr21:10954114..11002634hg19UCSC Ensembl
Innerchr21:9975985..10024505hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3848521
hg1948521
hg1848521
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057432
Supporting Variants
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)nssv3585058
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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