A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585642



Internal ID16373051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:15757441..15792231hg38UCSC Ensembl
Innerchr20:15738086..15772876hg19UCSC Ensembl
Innerchr20:15686086..15720876hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3834791
hg1934791
hg1834791
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7504n54
Supporting Variantsnssv938569
Samples
Known GenesMACROD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585642
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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