A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067359



Internal ID19156578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1581009..1617288hg38UCSC Ensembl
Innerchr20:1561655..1597934hg19UCSC Ensembl
Innerchr20:1509655..1545934hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3836280
hg1936280
hg1836280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4235n100
Supporting Variantsnssv3599113
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)nsv1067359
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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