A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066882



Internal ID19156101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:18682133..18708616hg38UCSC Ensembl
Innerchr21:20054451..20080934hg19UCSC Ensembl
Innerchr21:18976322..19002805hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3826484
hg1926484
hg1826484
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4392n100
Supporting Variantsnssv3599685
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1066882
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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