A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585682



Internal ID16373091
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:19924061..19924592hg38UCSC Ensembl
Innerchr20:19904705..19905236hg19UCSC Ensembl
Innerchr20:19852705..19853236hg18UCSC Ensembl
Cytoband20p11.23
Allele length
AssemblyAllele length
hg38532
hg19532
hg18532
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7511n54
Supporting Variantsnssv938624, nssv938626, nssv938631, nssv938625, nssv938635, nssv938628, nssv938632, nssv938621, nssv938636, nssv938620, nssv938630, nssv938629, nssv938627, nssv938634, nssv938622, nssv938633, nssv938623, nssv938619
Samples
Known GenesRIN2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585682
Frequency
Sample Size17421
Observed Gain10
Observed Loss8
Observed Complex0
Frequencyn/a


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