A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518598



Internal ID18816879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:105342384..105541309hg38UCSC Ensembl
Innerchr10:107102142..107301067hg19UCSC Ensembl
Innerchr10:107092132..107291057hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38198926
hg19198926
hg18198926
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1047422
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)nssv3518598
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