A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3664888



Internal ID18963169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12383639..12470001hg38UCSC Ensembl
Innerchr8:12241148..12327510hg19UCSC Ensembl
Innerchr8:12285519..12371881hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3886363
hg1986363
hg1886363
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021117
Supporting Variants
Samples
Known GenesDEFB109P1, FAM66A, FAM86B2, FAM90A25P, LOC100506990
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3664888
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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