A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3685566



Internal ID18983847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36397614..36578726hg38UCSC Ensembl
Innerchr8:36255132..36436244hg19UCSC Ensembl
Innerchr8:36374690..36555402hg18UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg38181113
hg19181113
hg18180713
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1021042
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3685566
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