A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3664653



Internal ID18962934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12382314..12454117hg38UCSC Ensembl
Innerchr8:12239823..12311626hg19UCSC Ensembl
Innerchr8:12284194..12355997hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3871804
hg1971804
hg1871804
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020355
Supporting Variants
Samples
Known GenesDEFB109P1, FAM66A, 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)nssv3664653
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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