A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1063406



Internal ID19152625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580922..1617678hg38UCSC Ensembl
Innerchr20:1561568..1598324hg19UCSC Ensembl
Innerchr20:1509568..1546324hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3836757
hg1936757
hg1836757
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4233n100
Supporting Variantsnssv3599044, nssv3599032, nssv3599017, nssv3734668, nssv3599022, nssv3599042, nssv3734670, nssv3599030, nssv3599028, nssv3599013, nssv3599019, nssv3599004, nssv3599023, nssv3599015, nssv3599026, nssv3599010, nssv3599043, nssv3599038, nssv3599024, nssv3599016, nssv3599040, nssv3599018, nssv3599003, nssv3599049, nssv3599008, nssv3599014, nssv3599005, nssv3599050, nssv3599045, nssv3599036, nssv3599029, nssv3599047, nssv3599025, nssv3734671, nssv3599020, nssv3599046, nssv3599035, nssv3599034, nssv3599033, nssv3599012, nssv3599041, nssv3599037, nssv3599007, nssv3734669, nssv3599006, nssv3599009, nssv3599021, nssv3599011, nssv3599039, nssv3599048, nssv3599027, nssv3599031
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)nsv1063406
Frequency
Sample Size11257
Observed Gain44
Observed Loss8
Observed Complex0
Frequencyn/a


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