A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3713285



Internal ID18664880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:95921392..96138605hg38UCSC Ensembl
Innerchr13:96573646..96790859hg19UCSC Ensembl
Innerchr13:95371647..95588860hg18UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38217214
hg19217214
hg18217214
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040320
Supporting Variants
Samples
Known GenesHS6ST3, UGGT2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3713285
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