A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685533



Internal ID18983814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:27965077..27991962hg38UCSC Ensembl
Innerchr8:27822594..27849479hg19UCSC Ensembl
Innerchr8:27878513..27905398hg18UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3826886
hg1926886
hg1826886
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1027577
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)nssv3685533
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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