A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064481



Internal ID19153700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580922..1609599hg38UCSC Ensembl
Innerchr20:1561568..1590245hg19UCSC Ensembl
Innerchr20:1509568..1538245hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3828678
hg1928678
hg1828678
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4230n100
Supporting Variantsnssv3596553, nssv3596557, nssv3596558, nssv3596555, nssv3596551, nssv3596560, nssv3596549, nssv3596552, nssv3596559, nssv3596554, nssv3730937, nssv3596550, nssv3596556, nssv3730938
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)nsv1064481
Frequency
Sample Size11257
Observed Gain14
Observed Loss0
Observed Complex0
Frequencyn/a


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