A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3594379



Internal ID18892660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580144..1613191hg38UCSC Ensembl
Innerchr20:1560790..1593837hg19UCSC Ensembl
Innerchr20:1508790..1541837hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3833048
hg1933048
hg1833048
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064634
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)nssv3594379
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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