A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3666869



Internal ID18965150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12403406..12616361hg38UCSC Ensembl
Innerchr8:12260915..12473870hg19UCSC Ensembl
Innerchr8:12305286..12518241hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38212956
hg19212956
hg18212956
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1022765
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)nssv3666869
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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