A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3583632



Internal ID18881913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10545409..10775598hg38UCSC Ensembl
Innerchr21:10736859..10967048hg19UCSC Ensembl
Innerchr21:9758730..9988919hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg38230190
hg19230190
hg18230190
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057621
Supporting Variants
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)nssv3583632
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer