A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv585229



Internal ID16372638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1578613..1601742hg38UCSC Ensembl
Innerchr20:1559259..1582388hg19UCSC Ensembl
Innerchr20:1507259..1530388hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3823130
hg1923130
hg1823130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7431n54
Supporting Variantsnssv935980, nssv936012, nssv935985, nssv935984, nssv935981, nssv935998, nssv936011, nssv935999, nssv936008, nssv935988, nssv935997, nssv936009, nssv935986, nssv935994, nssv935993, nssv936001, nssv935995, nssv936010, nssv936002, nssv936004, nssv935979, nssv936007, nssv936000, nssv935996, nssv935990, nssv935992, nssv935991, nssv936003, nssv935983, nssv936005, nssv935989, nssv935978, nssv935987, nssv936006, nssv935982
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv585229
Frequency
Sample Size17421
Observed Gain0
Observed Loss35
Observed Complex0
Frequencyn/a


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