A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064110



Internal ID19153329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10502083..10753328hg38UCSC Ensembl
Innerchr21:10759129..11010374hg19UCSC Ensembl
Innerchr21:9781000..10032245hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38251246
hg19251246
hg18251246
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4353n100
Supporting Variantsnssv3585011, nssv3585010
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)nsv1064110
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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