A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061567



Internal ID19150786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:11398836..11424654hg38UCSC Ensembl
Innerchr20:11379484..11405302hg19UCSC Ensembl
Innerchr20:11327484..11353302hg18UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3825819
hg1925819
hg1825819
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599377
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)nsv1061567
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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