A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060085



Internal ID19149304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580995..1617448hg38UCSC Ensembl
Innerchr20:1561641..1598094hg19UCSC Ensembl
Innerchr20:1509641..1546094hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3836454
hg1936454
hg1836454
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4235n100
Supporting Variantsnssv3599099
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)nsv1060085
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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