A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066711



Internal ID19155930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580129..1617288hg38UCSC Ensembl
Innerchr20:1560775..1597934hg19UCSC Ensembl
Innerchr20:1508775..1545934hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3837160
hg1937160
hg1837160
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4233n100
Supporting Variantsnssv3594320, nssv3594317, nssv3728477, nssv3594318, nssv3594319, nssv3594316
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)nsv1066711
Frequency
Sample Size11257
Observed Gain3
Observed Loss3
Observed Complex0
Frequencyn/a


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