A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066372



Internal ID19155591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580264..1591066hg38UCSC Ensembl
Innerchr20:1560910..1571712hg19UCSC Ensembl
Innerchr20:1508910..1519712hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3810803
hg1910803
hg1810803
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4234n100
Supporting Variantsnssv3594386
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)nsv1066372
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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