A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066051



Internal ID19155270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:38742206..38775439hg38UCSC Ensembl
Innerchr21:40114130..40147363hg19UCSC Ensembl
Innerchr21:39036000..39069233hg18UCSC Ensembl
Cytoband21q22.2
Allele length
AssemblyAllele length
hg3833234
hg1933234
hg1833234
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4431n100
Supporting Variantsnssv3600201, nssv3600200
Samples
Known GenesLINC00114
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066051
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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