A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060976



Internal ID19150195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580293..1609599hg38UCSC Ensembl
Innerchr20:1560939..1590245hg19UCSC Ensembl
Innerchr20:1508939..1538245hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3829307
hg1929307
hg1829307
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4230n100
Supporting Variantsnssv3595748, nssv3595745, nssv3595746, nssv3728566, nssv3595747
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)nsv1060976
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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