A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3760130



Internal ID19058411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12403406..12513862hg38UCSC Ensembl
Innerchr8:12260915..12371371hg19UCSC Ensembl
Innerchr8:12305286..12415742hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38110457
hg19110457
hg18110457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1018846
Supporting Variants
Samples
Known GenesFAM66A, 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)nssv3760130
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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