A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3647025



Internal ID18598620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:111069619..111091709hg38UCSC Ensembl
Innerchr5:110405317..110427407hg19UCSC Ensembl
Innerchr5:110433216..110455306hg18UCSC Ensembl
Cytoband5q22.1
Allele length
AssemblyAllele length
hg3822091
hg1922091
hg1822091
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1025735
Supporting Variants
Samples
Known GenesTSLP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3647025
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