A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3665761



Internal ID18964042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12389636..12555281hg38UCSC Ensembl
Innerchr8:12247145..12412790hg19UCSC Ensembl
Innerchr8:12291516..12457161hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38165646
hg19165646
hg18165646
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1034177
Supporting Variants
Samples
Known GenesDEFB109P1, FAM66A, 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)nssv3665761
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer