A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3745962



Internal ID19044243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:34156377..34234025hg38UCSC Ensembl
Innerchr5:34156482..34234130hg19UCSC Ensembl
Innerchr5:34192239..34269887hg18UCSC Ensembl
Cytoband5p13.2
Allele length
AssemblyAllele length
hg3877649
hg1977649
hg1877649
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1029078
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)nssv3745962
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