A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059730



Internal ID19148949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1566104..1581009hg38UCSC Ensembl
Innerchr20:1546750..1561655hg19UCSC Ensembl
Innerchr20:1494750..1509655hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3814906
hg1914906
hg1814906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3589971
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)nsv1059730
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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