A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065425



Internal ID19154644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580922..1591793hg38UCSC Ensembl
Innerchr20:1561568..1572439hg19UCSC Ensembl
Innerchr20:1509568..1520439hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3810872
hg1910872
hg1810872
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4232n100
Supporting Variantsnssv3596501, nssv3596502, nssv3596503
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)nsv1065425
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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