A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3734864



Internal ID19033145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1598463..1618926hg38UCSC Ensembl
Innerchr20:1579109..1599572hg19UCSC Ensembl
Innerchr20:1527109..1547572hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3820464
hg1920464
hg1820464
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1057460
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)nssv3734864
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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