A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3586439



Internal ID18538034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:13384193..14135181hg38UCSC Ensembl
Innerchr21:14756514..15507502hg19UCSC Ensembl
Innerchr21:13678385..14429373hg18UCSC Ensembl
Cytoband21q11.2
Allele length
AssemblyAllele length
hg38750989
hg19750989
hg18750989
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055396
Supporting Variants
Samples
Known GenesANKRD20A11P, C21orf15, LIPI, LOC100288966, MIR3156-3, MIR8069, POTED
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3586439
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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