A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059699



Internal ID19148918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1571458..1604463hg38UCSC Ensembl
Innerchr20:1552104..1585109hg19UCSC Ensembl
Innerchr20:1500104..1533109hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3833006
hg1933006
hg1833006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4225n100
Supporting Variantsnssv3589976
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)nsv1059699
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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