A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061382



Internal ID19150601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:22725403..22782562hg38UCSC Ensembl
Innerchr20:22706041..22763200hg19UCSC Ensembl
Innerchr20:22654041..22711200hg18UCSC Ensembl
Cytoband20p11.21
Allele length
AssemblyAllele length
hg3857160
hg1957160
hg1857160
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3584658
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)nsv1061382
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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