A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3596493



Internal ID18894774
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580341..1617288hg38UCSC Ensembl
Innerchr20:1560987..1597934hg19UCSC Ensembl
Innerchr20:1508987..1545934hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3836948
hg1936948
hg1836948
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055305
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)nssv3596493
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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