A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3728487



Internal ID19026768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580129..1618344hg38UCSC Ensembl
Innerchr20:1560775..1598990hg19UCSC Ensembl
Innerchr20:1508775..1546990hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3838216
hg1938216
hg1838216
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1065105
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)nssv3728487
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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