A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4367n100



Internal ID20155983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10420787..10558343hg38UCSC Ensembl
chr21:10954114..11091670hg19UCSC Ensembl
chr21:9975985..10113541hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38137557
hg19137557
hg18137557
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1056406, nsv1063484, nsv1060181, nsv1067343, nsv1059929
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)dgv4367n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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