A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061076



Internal ID19150295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:30185664..30271217hg38UCSC Ensembl
Innerchr20:29420340..29505893hg19UCSC Ensembl
Innerchr20:28034001..28119554hg18UCSC Ensembl
Cytoband20q11.1
Allele length
AssemblyAllele length
hg3885554
hg1985554
hg1885554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4294n100
Supporting Variantsnssv3584719, nssv3584720
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)nsv1061076
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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