A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3665966



Internal ID18964247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12403406..12555281hg38UCSC Ensembl
Innerchr8:12260915..12412790hg19UCSC Ensembl
Innerchr8:12305286..12457161hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38151876
hg19151876
hg18151876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028539
Supporting Variants
Samples
Known GenesFAM66A, FAM86B2, FAM90A25P, LOC100506990, LOC729732
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3665966
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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