A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065319



Internal ID19154538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10535770..10558343hg38UCSC Ensembl
Innerchr21:10954114..10976687hg19UCSC Ensembl
Innerchr21:9975985..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 Variantsdgv4364n100
Supporting Variantsnssv3585053
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)nsv1065319
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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