A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065006



Internal ID19154225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10576547..10753328hg38UCSC Ensembl
Innerchr21:10759129..10935910hg19UCSC Ensembl
Innerchr21:9781000..9957781hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38176782
hg19176782
hg18176782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4350n100
Supporting Variantsnssv3585002
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)nsv1065006
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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