A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3664841



Internal ID18963122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12382641..12720569hg38UCSC Ensembl
Innerchr8:12240150..12578078hg19UCSC Ensembl
Innerchr8:12284521..12622449hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38337929
hg19337929
hg18337929
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1030251
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)nssv3664841
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