A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062336



Internal ID19151555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1579309..1591545hg38UCSC Ensembl
Innerchr20:1559955..1572191hg19UCSC Ensembl
Innerchr20:1507955..1520191hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3812237
hg1912237
hg1812237
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4232n100
Supporting Variantsnssv3728373
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)nsv1062336
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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