A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3592726



Internal ID18891007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580129..1609876hg38UCSC Ensembl
Innerchr20:1560775..1590522hg19UCSC Ensembl
Innerchr20:1508775..1538522hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3829748
hg1929748
hg1829748
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064704
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)nssv3592726
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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