A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585641



Internal ID16373050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:15757441..15791937hg38UCSC Ensembl
Innerchr20:15738086..15772582hg19UCSC Ensembl
Innerchr20:15686086..15720582hg18UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg3834497
hg1934497
hg1834497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7504n54
Supporting Variantsnssv1152359
Samples1780862459_A
Known GenesMACROD2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585641
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer