A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059339



Internal ID19148558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1571784..1604463hg38UCSC Ensembl
Innerchr20:1552430..1585109hg19UCSC Ensembl
Innerchr20:1500430..1533109hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3832680
hg1932680
hg1832680
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4225n100
Supporting Variantsnssv3589982
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)nsv1059339
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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