A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065789



Internal ID19155008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1590128..1617678hg38UCSC Ensembl
Innerchr20:1570774..1598324hg19UCSC Ensembl
Innerchr20:1518774..1546324hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3827551
hg1927551
hg1827551
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4238n100
Supporting Variantsnssv3734814
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)nsv1065789
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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