A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060057



Internal ID18802588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:37963131..37992022hg38UCSC Ensembl
Innerchr21:39335434..39364324hg19UCSC Ensembl
Innerchr21:38257304..38286194hg18UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3828892
hg1928891
hg1828891
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3733448
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)nsv1060057
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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