A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3595914



Internal ID18894195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580341..1609599hg38UCSC Ensembl
Innerchr20:1560987..1590245hg19UCSC Ensembl
Innerchr20:1508987..1538245hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3829259
hg1929259
hg1829259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061367
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)nssv3595914
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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