A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3690085



Internal ID18641680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:142130048..142208924hg38UCSC Ensembl
Innerchr8:143211409..143290285hg19UCSC Ensembl
Innerchr8:143209316..143288192hg18UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3878877
hg1978877
hg1878877
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1016295
Supporting Variants
Samples
Known GenesLINC00051, MIR4472-1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3690085
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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