A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3596578



Internal ID18894859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580922..1609876hg38UCSC Ensembl
Innerchr20:1561568..1590522hg19UCSC Ensembl
Innerchr20:1509568..1538522hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3828955
hg1928955
hg1828955
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058095
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)nssv3596578
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer