A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3691541



Internal ID18989822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:131942683..132022170hg38UCSC Ensembl
Innerchr8:132954930..133034417hg19UCSC Ensembl
Innerchr8:133024112..133103599hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg3879488
hg1979488
hg1879488
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023761
Supporting Variants
Samples
Known GenesEFR3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3691541
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