A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3760176



Internal ID19058457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12403406..12709141hg38UCSC Ensembl
Innerchr8:12260915..12566650hg19UCSC Ensembl
Innerchr8:12305286..12611021hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38305736
hg19305736
hg18305736
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028761
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)nssv3760176
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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