A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067151



Internal ID18809682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:31374681..32180843hg38UCSC Ensembl
Innerchr21:32746995..33553155hg19UCSC Ensembl
Innerchr21:31668866..32475026hg18UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38806163
hg19806161
hg18806161
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3732695
Samples
Known GenesHUNK, LINC00159, SCAF4, SOD1, TIAM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067151
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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