A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589979



Internal ID18888260
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1571784..1591066hg38UCSC Ensembl
Innerchr20:1552430..1571712hg19UCSC Ensembl
Innerchr20:1500430..1519712hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3819283
hg1919283
hg1819283
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061826
Supporting Variants
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)nssv3589979
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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