A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067488



Internal ID19156707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1590079..1601434hg38UCSC Ensembl
Innerchr20:1570725..1582080hg19UCSC Ensembl
Innerchr20:1518725..1530080hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3811356
hg1911356
hg1811356
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4239n100
Supporting Variantsnssv3599222
Samples
Known GenesSIRPB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067488
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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