A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3589982



Internal ID18888263
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 StatusS
Merged Variantsnsv1059339
Supporting Variants
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)nssv3589982
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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