A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv586277



Internal ID16027000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:54037680..54044202hg38UCSC Ensembl
Innerchr20:52654219..52660741hg19UCSC Ensembl
Innerchr20:52087626..52094148hg18UCSC Ensembl
Cytoband20q13.2
Allele length
AssemblyAllele length
hg386523
hg196523
hg186523
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7612n54
Supporting Variantsnssv941567, nssv941568
Samples
Known GenesBCAS1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv586277
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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