A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3599098



Internal ID18897379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580995..1613191hg38UCSC Ensembl
Innerchr20:1561641..1593837hg19UCSC Ensembl
Innerchr20:1509641..1541837hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3832197
hg1932197
hg1832197
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1062208
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)nssv3599098
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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