A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4371n100



Internal ID20155987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10386269..10512961hg38UCSC Ensembl
chr21:10999496..11126188hg19UCSC Ensembl
chr21:10021367..10148059hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38126693
hg19126693
hg18126693
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058664, nsv1055647, nsv1064106, nsv1066400, nsv1066113, nsv1062409, nsv1056448
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)dgv4371n100
Frequency
Sample Size29084
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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