A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585227



Internal ID16372636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1578380..1591228hg38UCSC Ensembl
Innerchr20:1559026..1571874hg19UCSC Ensembl
Innerchr20:1507026..1519874hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3812849
hg1912849
hg1812849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7432n54
Supporting Variantsnssv935970
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585227
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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