A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3594329



Internal ID18892610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580129..1617678hg38UCSC Ensembl
Innerchr20:1560775..1598324hg19UCSC Ensembl
Innerchr20:1508775..1546324hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3837550
hg1937550
hg1837550
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058246
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)nssv3594329
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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