A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589973



Internal ID18888254
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 StatusS
Merged Variantsnsv1062968
Supporting Variants
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)nssv3589973
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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