A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065629



Internal ID19154848
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10548222..10611996hg38UCSC Ensembl
Innerchr21:10900461..10964235hg19UCSC Ensembl
Innerchr21:9922332..9986106hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3863775
hg1963775
hg1863775
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4357n100
Supporting Variantsnssv3585022
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)nsv1065629
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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