A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055518



Internal ID19144737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1571784..1587425hg38UCSC Ensembl
Innerchr20:1552430..1568071hg19UCSC Ensembl
Innerchr20:1500430..1516071hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3815642
hg1915642
hg1815642
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4224n100
Supporting Variantsnssv3589978
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)nsv1055518
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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