A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033112



Internal ID19122334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:133263632..133307532hg38UCSC Ensembl
Innerchr5:132599324..132643224hg19UCSC Ensembl
Innerchr5:132627223..132671123hg18UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3843901
hg1943901
hg1843901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648117
Samples
Known GenesFSTL4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033112
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