A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3585039



Internal ID18883320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:10534998..10579249hg38UCSC Ensembl
Innerchr21:10933208..10977459hg19UCSC Ensembl
Innerchr21:9955079..9999330hg18UCSC Ensembl
Cytoband21p11.1
Allele length
AssemblyAllele length
hg3844252
hg1944252
hg1844252
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059820
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)nssv3585039
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