A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585228



Internal ID16372637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1578380..1601742hg38UCSC Ensembl
Innerchr20:1559026..1582388hg19UCSC Ensembl
Innerchr20:1507026..1530388hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3823363
hg1923363
hg1823363
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7431n54
Supporting Variantsnssv935973, nssv935975, nssv935976, nssv935971, nssv935974, nssv935972, nssv935977
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585228
Frequency
Sample Size17421
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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