A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059827



Internal ID19149046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10558343..10775598hg38UCSC Ensembl
Innerchr21:10736859..10954114hg19UCSC Ensembl
Innerchr21:9758730..9975985hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38217256
hg19217256
hg18217256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4350n100
Supporting Variantsnssv3732400, nssv3732401, nssv3586006
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)nsv1059827
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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