A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062968



Internal ID19152187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1571458..1590116hg38UCSC Ensembl
Innerchr20:1552104..1570762hg19UCSC Ensembl
Innerchr20:1500104..1518762hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3818659
hg1918659
hg1818659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4224n100
Supporting Variantsnssv3589973
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)nsv1062968
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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