A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3515996



Internal ID18467591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:133429369..133559093hg38UCSC Ensembl
Innerchr10:135242873..135372597hg19UCSC Ensembl
Innerchr10:135092863..135222587hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38129725
hg19129725
hg18129725
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1038175
Supporting Variants
Samples
Known GenesCYP2E1, SCART1, SYCE1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3515996
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