A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997886



Internal ID18810736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:4294748..4373592hg38UCSC Ensembl
Innerchr3:4336432..4415276hg19UCSC Ensembl
Innerchr3:4311432..4390276hg18UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg3878845
hg1978845
hg1878845
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739581
Samples
Known GenesSETMAR, SUMF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997886
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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