A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056067



Internal ID19145286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:11193933..11233271hg38UCSC Ensembl
Innerchr20:11174581..11213919hg19UCSC Ensembl
Innerchr20:11122581..11161919hg18UCSC Ensembl
Cytoband20p12.2
Allele length
AssemblyAllele length
hg3839339
hg1939339
hg1839339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3599376
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)nsv1056067
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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