A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600085



Internal ID18898366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:26807463..26828391hg38UCSC Ensembl
Innerchr21:28179782..28200710hg19UCSC Ensembl
Innerchr21:27101653..27122581hg18UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg3820929
hg1920929
hg1820929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066328
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3600085
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