A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3600198



Internal ID18551793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38641811..38659757hg38UCSC Ensembl
Innerchr21:40013735..40031681hg19UCSC Ensembl
Innerchr21:38935605..38953551hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3817947
hg1917947
hg1817947
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055287
Supporting Variants
Samples
Known GenesERG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3600198
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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