A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4359n100



Internal ID22790446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10551998..10601230hg38UCSC Ensembl
chr21:10911227..10960459hg19UCSC Ensembl
chr21:9933098..9982330hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3849233
hg1949233
hg1849233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1058336, nsv1055153, nsv1066207
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)dgv4359n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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