A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3598999



Internal ID18897280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:1580922..1617448hg38UCSC Ensembl
Innerchr20:1561568..1598094hg19UCSC Ensembl
Innerchr20:1509568..1546094hg18UCSC Ensembl
Cytoband20p13
Allele length
AssemblyAllele length
hg3836527
hg1936527
hg1836527
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060078
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)nssv3598999
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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