A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055672



Internal ID19144891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1581009..1617678hg38UCSC Ensembl
Innerchr20:1561655..1598324hg19UCSC Ensembl
Innerchr20:1509655..1546324hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3836670
hg1936670
hg1836670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4235n100
Supporting Variantsnssv3734688
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)nsv1055672
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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