A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057475



Internal ID19146694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:19471246..19534698hg38UCSC Ensembl
Innerchr21:20843563..20907014hg19UCSC Ensembl
Innerchr21:19765434..19828885hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg3863453
hg1963452
hg1863452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3732673
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)nsv1057475
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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