A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055446



Internal ID19144665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1566104..1617288hg38UCSC Ensembl
Innerchr20:1546750..1597934hg19UCSC Ensembl
Innerchr20:1494750..1545934hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3851185
hg1951185
hg1851185
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4223n100
Supporting Variantsnssv3589972
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)nsv1055446
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