A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585686



Internal ID16373095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:19924112..19924613hg38UCSC Ensembl
Innerchr20:19904756..19905257hg19UCSC Ensembl
Innerchr20:19852756..19853257hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38502
hg19502
hg18502
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7511n54
Supporting Variantsnssv938762, nssv938742, nssv938746, nssv938757, nssv938755, nssv938743, nssv938749, nssv938751, nssv938756, nssv938758, nssv938763, nssv938761, nssv938738, nssv938740, nssv938768, nssv938766, nssv938739, nssv938741, nssv938748, nssv938750, nssv938753, nssv938765, nssv938752, nssv938747, nssv938744, nssv938759, nssv938767, nssv938760, nssv938745, nssv938754, nssv938764
Samples
Known GenesRIN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585686
Frequency
Sample Size17421
Observed Gain23
Observed Loss8
Observed Complex0
Frequencyn/a


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