A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685532



Internal ID18983813
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:27964180..27998854hg38UCSC Ensembl
Innerchr8:27821697..27856371hg19UCSC Ensembl
Innerchr8:27877616..27912290hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3834675
hg1934675
hg1834675
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016378
Supporting Variants
Samples
Known GenesSCARA5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3685532
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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