A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3686013



Internal ID18984294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:39441317..39526593hg38UCSC Ensembl
Innerchr8:39298836..39384112hg19UCSC Ensembl
Innerchr8:39417993..39503269hg18UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg3885277
hg1985277
hg1885277
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1032605
Supporting Variants
Samples
Known GenesADAM3A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3686013
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