A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055153



Internal ID19144372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10551998..10601230hg38UCSC Ensembl
Innerchr21:10911227..10960459hg19UCSC Ensembl
Innerchr21:9933098..9982330hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3849233
hg1949233
hg1849233
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4359n100
Supporting Variantsnssv3585028
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)nsv1055153
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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