A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586456



Internal ID18538051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:14244308..14282180hg38UCSC Ensembl
Innerchr21:15616629..15654501hg19UCSC Ensembl
Innerchr21:14538500..14576372hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg3837873
hg1937873
hg1837873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062532
Supporting Variants
Samples
Known GenesABCC13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3586456
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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