A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3675251



Internal ID18973532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:2473547..2725119hg38UCSC Ensembl
Innerchr8:2330755..2582660hg19UCSC Ensembl
Innerchr8:2318162..2570067hg18UCSC Ensembl
Cytoband8p23.2
Allele length
AssemblyAllele length
hg38251573
hg19251906
hg18251906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1028633
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)nssv3675251
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