A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv4364n100



Internal ID22790451
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:10535770..10558343hg38UCSC Ensembl
chr21:10954114..10976687hg19UCSC Ensembl
chr21:9975985..9998558hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3822574
hg1922574
hg1822574
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1057671, nsv1065319
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)dgv4364n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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